Dayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
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inquiryGood quantity Tungsten hexacarbonyl Basic information Product Name: Tungsten hexacarbonyl Synonyms: TUNGSTEN CARBONYL;(OC-6-11)-Tungstencarbonyl;(oc-6-11)-tungstencarbonyl(w(co)6;Hexac
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inquiryAbout Product Details Mol File: 14040-11-0.mol Tungsten hexacarbonyl Chemical Properties
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free samples NO.1 factory Tungsten hexacarbonyl Application:free samples NO.1 factory Tungsten hexacarbonyl
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inquirycarbon monoxide
1,2-bis-(diphenylphosphino)ethane
A
tungsten hexacarbonyl
B
[ Cu(1,2-bis(diphenylphosphino)ethane)2]BF4
Conditions | Yield |
---|---|
N2-atmosphere; 3 equiv. of phosphine; | A 60% B 99% |
Conditions | Yield |
---|---|
With carbon monoxide In diethyl ether High Pressure; under dried N2; addn. of N-methylbenzimine at 25°C to a soln. of W-complex (CO-pressure: 50 atm); stirring for 2 d at room temp., then for 1-2 h at 80-100°C; vac.-evapn. until dryness; residue dissolved in petroleum ether/ether; chromy. (silica gel/petroleum ether/ether); recrystn. from petroleum ether; elem. anal.; | A n/a B 96% |
With carbon monoxide In pentane High Pressure; under dried N2; addn. of N-methylbenzimine at 25°C to a soln. of W-complex (CO-pressure: 50 atm); stirring for 2 d at room temp., then for 1-2 h at 80-100°C; vac.-evapn. until dryness; residue dissolved in petroleum ether/ether; chromy. (silica gel/petroleum ether/ether); recrystn. from petroleum ether; elem. anal.; | A n/a B 96% |
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
With air In dichloromethane (N2); a soln. of W complex exposed to air for 120 min; evapd. (vac.), chromd. (silica, CH2Cl2); | A n/a B 96% |
Conditions | Yield |
---|---|
With carbon monoxide; water In acetone High Pressure; under nitrogen; autoclave: 50 atm CO-pressure, 70 h, room temperature;; evaporation, chromatography (silicagel, petroleum ether/ether), recrystd.; | A n/a B 95% |
tetrabutylammonium {1-η-trans-6-hydroxy-6,7,7-trimethyl-1-oxo-3-octen-1-yl}pentacarbonyltungstate(0)
triethyloxonium fluoroborate
A
tungsten hexacarbonyl
B
pentacarbonyl{ethoxy(trans-5-hydroxy-5,6,6-trimethyl-2-hepten-1-yl)carbene}tungsten
Conditions | Yield |
---|---|
In dichloromethane Ar atmosphere; stirring (0°C, 1 h); removal of solvent (vac.), addn. of n-hexane, stirring (1 h), filtration, pptn. of W(CO)6 on concn. and cooling (-30°C), decantation, evapn. of soln. to dryness; | A n/a B 91% |
(tungstenpentacarbonyl)2(μ-CH3OCCH(C3H7)CH2C(CH3)(CH2CHCH2)COCH3)
A
tungsten hexacarbonyl
B
(η(6)-benzene)tungsten(0) tricarbonyl
Conditions | Yield |
---|---|
In benzene-d6 heating 3 h in benzene at 75°C; identification of organometallic products by (13)C NMR; | A n/a B n/a C 90% |
In benzene heating 3 h in benzene at 75°C; identification of organometallic products by (13)C NMR; | A n/a B n/a C 90% |
benzylidene phenylamine
A
tungsten hexacarbonyl
D
triphenylhydroxysilane
Conditions | Yield |
---|---|
With carbon monoxide In diethyl ether High Pressure; under dried N2; addn. of N-methylbenzimine at 25°C to a soln. of W-complex (CO-pressure: 50 atm); stirring for 2 d at room temp., then for 1-2 h at 80-100°C; vac.-evapn. until dryness; residue dissolved in petroleum ether/ether; chromy. (silica gel/petroleum ether/ether); recrystn. from petroleum ether; elem. anal.; | A n/a B n/a C n/a D 90% |
dicobalt octacarbonyl
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In petroleum ether MoW(CC6H4Me-4)(CO)7(C5H5) in light petroleum treated with Co2(CO)8, refluxed for 1 h; evapd. in vac., chromd. (Al2O3, CH2Cl2-light petroleum (1:4)), evapd. in vac.; elem. anal.; | A n/a B 90% |
pentacarbonyl{4-cycloheptatrienyl-1-(diethylamino)-3-ethoxy-2-methyl-2E-butenylidene}tungsten
A
tungsten hexacarbonyl
B
(pentacarbonyl)(diethylamino)tungsten
Conditions | Yield |
---|---|
In toluene byproducts: 3-ethoxy-2-methyl-5H-benzocycloheptatriene, 2-ethoxy-3-methyl-5H-benzocycloheptatriene, 2-ethoxy-3-methyl-7H-benzocycloheptatriene; inert atmosphere; heating (5 h, 100°C); chromy. (silica gel, petroleum ether/CH2Cl2 4:1); elem. anal.; | A n/a B 88% |
pentacarbonyl{2-(cyclohepta-2,4,6-trien-1-yl)-1-ethoxyethylidene}tungsten
(E)-N,N-dimethylcinnamamide
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
With phosphorus oxychloride; triethylamine In dichloromethane under Ar atm. to N,N-dimethyl-3-phenylacrylamide in CH2Cl2 was added POCl3 and stirred at 0°C for 30 min, W complex and NEt3 in CH2Cl2 were added, 20°C, 16 h; react. mixt. was evapd. at 20°C, residue was dissolved in CH2Cl2 and chromed. on silica; diastereomers were not isolated; | A n/a B 86% |
2Na(1+)*W(CO)5(2-) = Na2[W(CO)5]
carbon dioxide
A
tungsten hexacarbonyl
B
sodium carbonate
Conditions | Yield |
---|---|
In tetrahydrofuran reductive disproportionation; mechanism discussed;; IR;; | A 83% B n/a |
In tetrahydrofuran soln. of the W-compound was treated with gasous CO2 at -78°C, warmed to 25°C; solvent removed (vac.), extd. (diethyl ether), ether removed (vac.); IR, MAS; | A 83% B n/a |
Conditions | Yield |
---|---|
In tetrahydrofuran reductive disproportionation; mechanism discussed;; IR;; | A 82% B 74% |
In tetrahydrofuran soln. of the W-compound was treated with gasous CO2 at -78°C, warmed to 25°C; solvent removed (vac.), extd. (diethyl ether), ether removed (vac.); IR, MAS; | A 82% B 74% |
(CO)5WOs(CO)4(P(CH3)3)
A
tungsten hexacarbonyl
B
osmium(carbonyl)4(P(methyl)3)
Conditions | Yield |
---|---|
In benzene Irradiation (UV/VIS); irradn. (λ > 400 nm); detd. by IR spectroscopy; | A 66% B 82% |
(CO)5WOs(CO)4(P(CH3)3)
triphenylphosphine
A
tungsten hexacarbonyl
B
triphenylphosphine tungsten pentacarbonyl
C
Os(CO)3(P(CH3)3)(P(C6H5)3)
D
osmium(carbonyl)4(P(methyl)3)
Conditions | Yield |
---|---|
In benzene Irradiation (UV/VIS); irradn. (λ > 400 nm); detd. by IR spectroscopy; | A 8% B 81% C 49% D 46% |
dimethyl amine
A
tungsten hexacarbonyl
B
pentacarbonyl-dimethylamine-tungsten
Conditions | Yield |
---|---|
In dichloromethane byproducts: 5,5'-diphenyl-2,2'-bifuran; Ar atmosphere, addn. of Me2NH to soln. of W complex at -78°C, warming to room temp., stirring (1 d); removement of solvent, column chromy. (silica gel, elution of W(CO)6 andorganic byproduct with petroleum ether (fraction 40.60°C)/CH2Cl2 (3:1), elution of (Me2NH)W(CO)5 with petroleum ether (fraction 40-60.de gree.C)/CH2Cl2 (1:1)); | A 8% B 80% |
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
With CO In petroleum ether light petroleum soln. of Rh(C2H4)2(C9H7) treated with CO gas (15 min), solid CoW(CC6H4Me-4)(CO)8 added, stirred for 12 h; evapd. in vac., chromd. (Al2O3, CH2Cl2-light petroleum (1:2)), evapd. in vac., crystd. from CH2Cl2-light petroleum (1:10); elem. anal.; | A n/a B 80% C <1 |
2-ethynyl-quinoline
tungsten pentacarbonyl tetrahydrofuran
triethyloxonium fluoroborate
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
With n-BuLi In dichloromethane under N2 or Ar; n-BuLi in hexane added (-80°C) to alkyne in THF; stirred (-80°C, 20 min); W complex in THF added; stirred (ambienttemp., 30 min); solvent removed; dissolved in CH2Cl2; treated with Et3O BF4 (0°C); stirred (60 min); filtered at -20°C through silica layer using CH2Cl2 as eluent; solvent evapd.; sepd. by chromy. (silica, -20°C, pentane-CH2Cl2 2:1, 1:1 to 1:3); elem. anal.; | A n/a B 80% |
triphenylphosphine
A
tungsten hexacarbonyl
B
W(CO)4((C6H5)3P)2
C
triphenylphosphine tungsten pentacarbonyl
Conditions | Yield |
---|---|
In benzene-d6 thermal decompn. (45°C/6 h/sealed tube);; (CO)5WPPh3 isolated by thin layer chromy. (SiO2/hexane);; | A n/a B n/a C 79% D n/a E n/a |
Conditions | Yield |
---|---|
In tetrahydrofuran reductive disproportionation;; IR;; | A 48% B 78% |
B
tungsten hexacarbonyl
C
(C2H5)2NCHC(N(C2H5)2)CH(C6H5)2
Conditions | Yield |
---|---|
With carbon monoxide In diethyl ether (CO)5WTeC(Ph)C(NEt2)CPh2 in ether with CO pressure of 100 bar, 18 h at 60°C; chromy. (silicagel, pentane/CH2Cl2) at -20°C; | A n/a B n/a C 77% |
(cyclohexyl)2PCH2CH2PPh2
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran heating at reflux, 40 min; warming under vac. (removal of solvent and W(CO)6), chromy. over a silica column with 3:1 benzene-hexane, elem. anal.; | A n/a B 75% |
methyl(diethylamino)acetylene
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In dichloromethane under N2, 40 min at 0°C; removal of solvent in vac., chromy. on silica gel (petroleum ether/CH2Cl2 (2:1), 0°C), removal of solvent in vac., recrystn. (petroleum ether/toluene 5:1); elem. anal.; | A n/a B 75% C 10% |
N-Benzylidenemethylamine
A
tungsten hexacarbonyl
D
triphenylhydroxysilane
Conditions | Yield |
---|---|
With carbon monoxide In diethyl ether High Pressure; under dried N2; addn. of N-methylbenzimine at 25°C to a soln. of W-complex (CO-pressure: 50 atm); stirring for 2 d at room temp., then for 1-2 h at 80-100°C; vac.-evapn. until dryness; residue dissolved in petroleum ether/ether; chromy. (silica gel/petroleum ether/ether); recrystn. from petroleum ether; elem. anal.; | A n/a B 74% C 16% D 5% |
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) slow heating of carbene complex in a Schlenk tube at 2.00 Torr and 110°C, melting with formation of bubbles; pptn. of W(CO)6 on cool parts of tube, dissolution of melt in ether/petroleum ether, chromy. on silica at -20°C with ether/petroleum ether, elution of orange part with ether, spect. detected; | A n/a B 74% |
1,10-Phenanthroline
A
tungsten hexacarbonyl
B
bis(pentacarbonyltungsten)(1,10-phenanthroline)tin
C
tetracarbonyl(1,10-phenanthroline)tungsten(0)
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: NaCl; Ar atmosphere, addn. of solid ligand to THF soln. of metal complex at 20°C, stirring (20°C, 30 min); removement of solvent (vacuum), dissolution (THF), chromy. (silica gel, elution of byproducts with Et2O, elution of main product with THF), evapn. to dryness; elem. anal.; | A n/a B 71% C n/a |
2-ethynyl-quinoline
tungsten pentacarbonyl tetrahydrofuran
trimethoxonium tetrafluoroborate
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
With n-BuLi In dichloromethane under N2 or Ar; n-BuLi in hexane added (-80°C) to alkyne in THF; stirred (-80°C, 20 min); W complex in THF added; stirred (ambienttemp., 30 min); solvent removed; dissolved in CH2Cl2; treated with Me3O BF4 (0°C); stirred (60 min); filtered at -20°C through silica layer using CH2Cl2 as eluent; solvent evapd.; sepd. by chromy. (silica, -20°C, pentane-CH2Cl2 2:1, 1:1 to 1:3); elem. anal.; | A n/a B 71% |
Conditions | Yield |
---|---|
In dichloromethane under N2, complex in CH2Cl2 was refluxed for 4 h; soln. was evapd., residue was chromd.; products were analized by NMR, IR; | A n/a B n/a C 70% |
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) slow heating of carbene complex in a Schlenk tube at 0.50 Torr and 125°C, melting with formation of bubbles; pptn. of W(CO)6 on cool parts of tube, dissolution of melt in ether/petroleum ether, chromy. on silica at -20°C with ether/petroleum ether, elution of orange part with ether, recrystn. from ether/pentane, elem. anal.; | A n/a B 70% |
tungsten pentacarbonyl tetrahydrofuran
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: Me2S; under N2; W-complex in THF added to Fe-complex in THF, stirred overnight at room temp.; dried (vac.), dissolved in CH2Cl2, chromy. (alumina; eluent: CH2Cl2:petrolether = 1:1 (v/v)), crystn.; | A n/a B 70% C n/a |
A
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In dichloromethane CH2Cl2, 20°C, 1.5 h; flash chromy. (silica gel, pentane/diethylether (1/1)); elem. anal.; | A n/a B 69% |
In (2)H8-toluene toluene-d8, 30°C, 1 h; not sepd., detected by NMR spectroscopy; |
tungsten hexacarbonyl
1,1',3,3'-tetramethyl-2,2'-biimidazolidinylidene
cis-tetracarbonylbis(1,3-dimethyl-4-imidazolidin-2-ylidene)tungsten(0)
Conditions | Yield |
---|---|
In decalin byproducts: CO; inert atmosphere; excess olefin, > 180°C; elem. anal.; | 100% |
tungsten hexacarbonyl
acetonitrile
bis(acetonitrile)diiodotricarbonyltungsten(II)
Conditions | Yield |
---|---|
With iodine In acetonitrile under Ar, a suspension of W(CO)6 in NCCH3 refluxed (72 h), cooled (0°C), I2 added; solvent removed (vac.), crystn.; elem. anal.; | 100% |
tungsten hexacarbonyl
benzyl azide
(bezylisocyanide)pentacarbonyltungsten
Conditions | Yield |
---|---|
With triphenylphosphine In tetrahydrofuran stirring, 25°C, 10 h; | 100% |
tungsten hexacarbonyl
1,2-bis-(diphenylphosphino)ethane
A
tetracarbonyl-1,2-bis(diphenylphosphino)ethane-tungsten(0)
B
{μ-bis(diphenylphosphino)ethane}-bis{pentacarbonyltungsten(0)}
Conditions | Yield |
---|---|
With trimethylamine-N-oxide In acetonitrile W(CO)6 and Me3NO stirred in MeCN (20°C, 30 min, under nitrogen), addn. of diphosphine (molar ratio W(CO)6 : phosphine = 2:1), heated (75°C, 16 h), soln. pumped to dryness; washed with hexane; 31P-NMR; | A 0% B 100% |
tungsten hexacarbonyl
2,2'-Bipyrimidine
(μ-2,2'-bipyrimidine){W(CO)4}2
Conditions | Yield |
---|---|
In xylene mixt. W(CO)6 and bpym in xylene heated at reflux for 4 h under N2; soln. cooled to room temp., crystals filtered, washed with acetonitrileand petroleum ether and dried under vac.; elem. anal.; | 100% |
tungsten hexacarbonyl
2-(2-pyridyl)-4-(4-fluorophenyl)-6-phenylphosphinine
2-(2-pyridyl)-4-phenyl-6-(4-fluorophenyl)phosphinine-P,N-tungsten tetracarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 UV-irradiation; Inert atmosphere; Sealed tube; | 100% |
In tetrahydrofuran-d8 UV-irradiation; |
tungsten hexacarbonyl
2-(2-pyridyl)-4-(4-trifluoromethylphenyl)-6-phenylphosphinine
2-(2-pyridyl)-4-phenyl-6-(4-trifluoromethylphenyl)phosphinine-P,N-tungsten tetracarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 UV-irradiation; Inert atmosphere; Sealed tube; | 100% |
In tetrahydrofuran-d8 UV-irradiation; |
tungsten hexacarbonyl
2-(2-pyridyl)-4-(4-methylthiophenyl)-6-phenylphosphinine
2-(2-pyridyl)-4-phenyl-6-(4-methylthiophenyl)phosphinine-P,N-tungsten tetracarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 UV-irradiation; Inert atmosphere; Sealed tube; | 100% |
In tetrahydrofuran-d8 UV-irradiation; |
tungsten hexacarbonyl
2-(2-pyridyl)-4,6-diphenylphosphinine-P,N-tungsten tetracarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 UV-irradiation; Inert atmosphere; Sealed tube; | 100% |
In tetrahydrofuran-d8 at 20℃; for 12h; Inert atmosphere; Schlenk technique; Glovebox; UV-irradiation; | 58% |
In tetrahydrofuran-d8 UV-irradiation; | |
In toluene at 120℃; Inert atmosphere; Schlenk technique; Glovebox; |
tungsten hexacarbonyl
4,6-diphenyl-[2,2']bipyridinyl
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 for 24h; UV-irradiation; Inert atmosphere; Sealed tube; | 100% |
In tetrahydrofuran-d8 at 20℃; for 48h; Inert atmosphere; Schlenk technique; Glovebox; UV-irradiation; | 70% |
In toluene at 120℃; Inert atmosphere; Schlenk technique; Glovebox; |
tungsten hexacarbonyl
Conditions | Yield |
---|---|
With sodium tetrahydroborate; dichloromethane In ethanol N2; addn. of 10.0 mmol W(CO)6, 10.0 mmol ligand and 60.3 mmol NaBH4 to hot ethanol; refluxing for 14 h; removal of C2H5OH; shaking with H2O/CH2Cl2; separation of CH2Cl2 layer;drying over MgSO4; filtration; evapn. to dryness; elem. anal.; | 99.2% |
With sodium tetrahydroborate; dichloromethane In ethanol N2; addn. of 10.0 mmol W(CO)6, 10.0 mmol ligand and 60.3 mmol NaBH4 to hot ethanol; refluxing for 14 h; removal of C2H5OH; shaking with H2O/CH2Cl2; separation of CH2Cl2 layer;drying over anhydrous MgSO4; filtration; evapn. to dryness; refluxing in CH2Cl2 under N2; addn. of hexane; evapn. till slight cloudiness; cooling to -10°C; elem. anal.; | 78% |
Conditions | Yield |
---|---|
In further solvent(s) air-free techniques; refluxed; | 99% |
tungsten hexacarbonyl
tris(2-pyridyl)methane
(tri-2-pyridylmethane)tricarbonyltungsten
Conditions | Yield |
---|---|
In acetonitrile N2 atmosphere; refluxing of W(CO)6 in MeCN (48 h), addn. of ligand, refluxing (12 h); sepn. (decantation), washing (CH2Cl2), drying (vac., overnight); elem. anal.; | 99% |
tungsten hexacarbonyl
acetone
1,2-bis-(diphenylphosphino)ethane
fac-[W(CO)3(1,2-bis(diphenylphosphino)ethane)(Me2CO)]
Conditions | Yield |
---|---|
In acetone Irradiation (UV/VIS); N2-atmosphere; irradn. (450 W Hg lamp, 10 h); evapn. (vac.), washing (hexane / Et2O = 3 : 1), drying (vac.); | 99% |
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran a THF-soln. of W(CO)6 was added at room temp. to a dispersion of Ti-complex in THF, the mixt. was warmed at 70°C for 4 days, cooled (N2); filtered, the solvent and an excess of W(CO)6 were removed in vac., extd. with CH3CN, cooled to -20°C; elem. anal.; | 99% |
tetrahydrofuran
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran Irradiation (UV/VIS); (N2); a soln. of W complex irradiated with a Hg lamp for 2.5 h, a soln. of ligand added, stirred overnight; THF-removed (vac.), dissolved in CHCl3, passed through a silica gel column, chromd. (GPC); elem. anal.; | 99% |
((CH3)2NB)2(NC6H3(CH(CH3)2)2)2C
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In benzene Irradiation (UV/VIS); C6H6, UV-promoted; crystd. from benzene; | 99% |
tetrahydrofuran
tungsten hexacarbonyl
(CO)5W(P(CH2NMe)3P)
(CO)5W(P(CH2NMe)3P)W(CO)5
Conditions | Yield |
---|---|
In tetrahydrofuran Irradiation (UV/VIS); irradiation of THF soln. of tungsten hexacarbonyl for 12 h with 450 W water cooled UV immersion lamp, addn. to stirred soln. of phosphorus compd. in THF, stirring for 24 h; evapn., heating at 70°C at 300 mTorr, dissolving in THF, addn. ofpentane, filtration, drying in vac., elem. anal.; | 99% |
tetrahydrofuran
2,6-diisocyano-1,3-diethoxycarbonylazulene
tungsten hexacarbonyl
[(OC)5W(2,6-diisocyano-1,3-diethoxycarbonylazulene)W(CO)5]
Conditions | Yield |
---|---|
In tetrahydrofuran Irradiation (UV/VIS); (Ar); a soln. of W complex photolyzed, added to a soln. of ligand dropwise at room temp., stirred; evapd. (vac.), sublimed at 1E-2 Torr at 40°C, chromd. (silica gel, CHCl3), solvent-removed, dried at 1E-2 Torr; elem. anal.; | 99% |
tungsten hexacarbonyl
8,16,24,32-tetraisocyano[2.2.2.2]metacyclophane
[(CO)5W]4(μ4-η1:η1:η1:η1-8,16,24,32-tetraisocyano[2.2.2.2]metacyclophane)
Conditions | Yield |
---|---|
With THF In tetrahydrofuran Irradiation (UV/VIS); (Ar); soln. of W complex in THF was photolyzed for 4 h; transferred dropwise to soln. of ligand at room temp.; stirred for 15 h; solvent removed (vac.); chromd. (silica gel, CH2Cl2); solvent removed; dried (vac.); elem. anal.; | 99% |
Conditions | Yield |
---|---|
With tBuOK In tetrahydrofuran byproducts: CO; at room temp.; NMR, IR; | 99% |
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In tetrahydrofuran at room temp.; NMR, IR; | 99% |
tungsten hexacarbonyl
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane (Ar); refluxing 1:1 mixt. of potassium cyclopentadienide and tungsten compd. in DME for 40 h; filtration, evapn., addn. of hexane, sonication, evapn., drying at 50°C in vac. for 4 h, NMR and IR; | 99% |
tungsten hexacarbonyl
N-methyl-N-nitrosotoluene-p-sulfonamide
Conditions | Yield |
---|---|
Stage #1: tungsten hexacarbonyl; C12H19Na In tetrahydrofuran at 78℃; for 96h; Stage #2: N-methyl-N-nitrosotoluene-p-sulfonamide In tetrahydrofuran for 2h; | 99% |
tungsten hexacarbonyl
4-chlorobenzonitrile
carbonic acid dimethyl ester
N-(4-chlorophenyl)acetamide
Conditions | Yield |
---|---|
With di(rhodium)tetracarbonyl dichloride; 1,3-bis-(diphenylphosphino)propane; sodium phosphate; sodium iodide In water at 120℃; for 24h; Inert atmosphere; Sealed tube; | 99% |
tungsten hexacarbonyl
1-methyl-3-nitrobenzene
carbonic acid dimethyl ester
3-Methylacetanilide
Conditions | Yield |
---|---|
With di(rhodium)tetracarbonyl dichloride; 1,3-bis-(diphenylphosphino)propane; sodium phosphate; sodium iodide In water at 120℃; for 24h; Inert atmosphere; Sealed tube; | 99% |
tungsten hexacarbonyl
carbonic acid dimethyl ester
1-ethoxy-4-nitrobenzene
4-ethoxyacetanilide
Conditions | Yield |
---|---|
With di(rhodium)tetracarbonyl dichloride; 1,3-bis-(diphenylphosphino)propane; sodium phosphate; sodium iodide In water at 120℃; for 24h; Inert atmosphere; Sealed tube; | 99% |
tungsten hexacarbonyl
trans-triphenylphosphane tetracarbonyltungsten
Conditions | Yield |
---|---|
With triphenylphosphine In ethanol; water under N2, W(CO)6, NaBH4 and PPh3 suspended in 95%EtOH at room temp., mixt. refluxed and stirred vigorously for 12h; cooled, filtered, washed (water, hot EtOH, acetone, pentane); | 98% |
tungsten hexacarbonyl
iodine(I) bromide
acetonitrile
WBrI(CO)3(NCCH3)2
Conditions | Yield |
---|---|
In acetonitrile N2-atmosphere; refluxing of W(CO)6 (72 h), then BrI addn. at 0°C, stirring (30 min); solvent evapn. (vac.); elem. anal.; | 98% |
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