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2,2-dimethylpropaneAppearance:ask Storage:Keep in dry and cool condition Package:foil aluminium bag/vacuum packing Application:intermediates Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airport)
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high purity Application:Drug intermediates Materials intermediates and active molecules
2,2-dimethylpropane
Conditions | Yield |
---|---|
In benzene-d6 Kinetics; thermolysis at 167 +/- 1°C; | 100% |
trans-neopentyl(trifluoromethanesulfonato)bis(trimethylphosphine)platinum(II)
toluene
C
2,2-dimethylpropane
D
1,1-dimethylcyclopropane
Conditions | Yield |
---|---|
In toluene Kinetics; thermolysis in toluene at 133°C for 80 min (Ar or N2); | A n/a B n/a C 99% D 1% |
methane
[(η5-pentamethylcyclopentadienide)Sc(CH2C(CH3)3]
A
(eta.5-C5Me5)2ScCH3
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In Cyclohexane-d12 Kinetics; under Ar, in the dark; in NMR tube; CH4 added to soln. of Sc complex in cyclohexane-d12 at 77 K; warmed to 11-50°C; not isolated; monitored by (1)H NMR spectra; | A 99% B 99% |
In benzene-d6 Kinetics; under Ar, in the dark; in NMR tube; CH4 added to soln. of Sc complex in benzene-d6 at 77 K; warmed to 11-50°C; not isolated; monitored by (1)H NMR spectra; | A 99% B 99% |
Conditions | Yield |
---|---|
In diethyl ether under Ar; soln. of t-BuOH in Et2O added to In compd. (molar ratio 1:1) in Et2O at room temp.; stirred for 1 h; volatiles removed by vac. distn.; recrystd. from Et2O at -40°C; crystals washed with pentane at 0°C; elem. anal.; | A 0% B 98.3% |
2,2-dimethylpropane
Conditions | Yield |
---|---|
With hydrogenchloride In toluene protonolysis with gaseous HCl; | 98% |
Conditions | Yield |
---|---|
In Cyclopentane; cyclohexane (Ar); a soln. of Pt-complex heated at 150°C for 24 min; quenched thermally at -196°C; evapd.; dissolved in acetonitrile;separated; evapd.; | A 98% B n/a |
trineopentylaluminum*H2NCH3
A
dineopentylaluminum(CH3NH)
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In neat (no solvent) Freshly sublimed ((CH3)3CCH2)3Al*CH3NH2 is heated under protective gas for 10 h at 96°C.; After cooling distn. of neopentane, vac. sublimation of residue at 80°C, elem. anal., mol wt.; | A 97% B n/a |
3-methyl-2-isopropyl-1-butene
A
{3-methyl-2-(2-propyl)-1-butene}{bis(dicyclohexylphosphino)ethane}platinum(0)
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In cyclohexane Kinetics; thermolysis of cis-hydridoneopentyl{bis(dicyclohexylphosphino)ethane}platinum(II) in 3-methyl-2-(2-propyl)-1-butene/cyclohexane via supposed {bis(dicyclohexylphosphino)ethane}platinum(0) at 69°C to completion; | A 97% B n/a |
trineopentylindium
diphenylphosphane
A
((CH3)3CCH2)2In(P(C6H5)2)
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In benzene The mixt. of reagents in benzene was kept at 60°C for 3 d;; evapd., washed with benzene, pentane at -78°C;; | A 69.3% B 96.6% |
Conditions | Yield |
---|---|
With hydrogen; silica gel; palladium at 330℃; | 96% |
tert-butylethylene
A
(3,3-dimethyl-1-butene){bis(dicyclohexylphosphino)ethane}platinum(0)
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In cyclohexane Kinetics; thermolysis of cis-hydridoneopentyl{bis(dicyclohexylphosphino)ethane}platinum(II) in 3,3-dimethyl-1-butene/cyclohexane via supposed {bis(dicyclohexylphosphino)ethane}platinum(0) at 69°C for 2.2 h; | A >99 B 96% |
2,2-dimethylpropane
Conditions | Yield |
---|---|
With hydrogenchloride In toluene protonolysis with gaseous HCl; | 96% |
Conditions | Yield |
---|---|
In dichloromethane at 0℃; for 1h; | 95% |
2,3-Dimethyl-2-butene
A
(2,3-dimethyl-2-butene){bis(dicyclohexylphosphino)ethane}platinum(0)
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In cyclohexane Kinetics; thermolysis of cis-hydridoneopentyl{bis(dicyclohexylphosphino)ethane}platinum(II) in 2,3-dimethyl-2-butene/cyclohexane via supposed {bis(dicyclohexylphosphino)ethane}platinum(0) at 69°C to completion; | A 94% B >99 |
tricyclohexylphosphine
A
(tricyclohexylphosphine){bis(dicyclohexylphosphino)ethane}platinum(0)
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In cyclohexane Kinetics; thermolysis of cis-hydridoneopentyl{bis(dicyclohexylphosphino)ethane}platinum(II) in tricyclohexylphosphine/cyclohexane via supposed {bis(dicyclohexylphosphino)ethane}platinum(0) at 68.9°C to completion; | A 94% B >99 |
2,2-dimethylpropane
Conditions | Yield |
---|---|
With sulfuric acid -10°C; GLC; | 93% |
neopentyl iodide
A
2,2,5,5-tetramethylhexane
B
2,2-dimethylpropane
C
1,1-dimethylcyclopropane
Conditions | Yield |
---|---|
With tetrabutylammonium perchlorate; nickel(II) perchlorate; triphenylphosphine In acetonitrile at 25℃; | A 92% B 2.5% C 2.5% |
Conditions | Yield |
---|---|
With titanium tetrachloride In dichloromethane at 0℃; for 3h; | 90% |
neopentyl(η5-pentamethylcyclopentadienyl)bis(trimethylphosphine)ruthenium
toluene
A
(η5-pentamethylcyclopentadienyl)-m-tolylbis(trimethylphosphine)ruthenium
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In toluene Ar atmosphere, 60°C, 24 h; volatiles removal (vacuum); | A 90% B n/a |
tetramethylsilane
cis-hydrido(trimethylsilylmethyl){bis(dicyclohexylphosphino)ethane}platinum(II)
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In cyclohexane Kinetics; thermolysis of cis-hydridoneopentyl{bis(dicyclohexylphosphino)ethane}platinum(II) in tetramethylsilane/cyclohexane via supposed {bis(dicyclohexylphosphino)ethane}platinum(0) at 69.8°C for 3 h; | A 85% B 83% |
trans-neopentyl(trifluoromethanesulfonato)bis(trimethylphosphine)platinum(II)
benzene-d6
B
2,2-dimethylpropane
C
neopentane-d1
D
1,1-dimethylcyclopropane
Conditions | Yield |
---|---|
In benzene-d6 Kinetics; react. in a sealed 5-mm NMR tube, 133°C, 80 min (2 half-lives) (Ar or N2); | A n/a B 14% C 83% D 3% |
Conditions | Yield |
---|---|
In toluene inert atmosphere, -35°C, 70 h; pptn. of complex (hexane addn.), recrystn. (toluene/hexane); elem. anal.; | A 12% B 83% C 7.3% |
A
1,5-cis,cis-cyclooctadiene
B
2,2,5,5-tetramethylhexane
C
2,2-dimethylpropane
D
(1Z,3Z,5Z)-Cycloocta-1,3,5-triene
Conditions | Yield |
---|---|
With tris(1-methylethyl)phosphine In Cyclopentane; cyclohexane 50 deg C,15 h; 126 deg C, 2 h; Further byproducts given; | A 80% B 36 % Chromat. C 106 % Chromat. D 14 % Chromat. |
trineopentylaluminum*P(Ph2)H
A
dineopentylaluminum{Ph2phosphide}
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
Trineopentylaluminum*P(Ph)2H is heated under protective gas at 180°C for 24 h.; Resulting solid Al-compd. is washed with pentane.; | A 78% B n/a |
cis-dioxo ReO2(CH2CMe3)3
A
ReO2(CH2tBu)(neopentylidene)
B
2,2-dimethylpropane
Conditions | Yield |
---|---|
In pyridine Irradiation (UV/VIS); photolysis for 1 h, using Pyrex glass-filtered light from a medium pressure mercury lamp;; Re-complex and neopentane were the only identifiable products, isolation of Re-complex by sublimation (40 ° C/ 10 E-4 torr); | A 76% B n/a |
In acetonitrile Irradiation (UV/VIS); photolysis for 1 h, using Pyrex glass-filtered light from a medium pressure mercury lamp;; isolation of Re-complex by sublimation (40 ° C/ 10 E-4 torr); |
A
2,2-dimethylpropane
B
ethene
C
1,1-dimethylcyclopropane
D
3-Methyl-1-butene
E
isobutene
Conditions | Yield |
---|---|
In toluene inert atmosphere, thermal decompn. (85°C); GLC; | A 5% B 5% C 74% D 4% E 12% |
A
methane
B
2,2-dimethylpropane
C
methylbutane
D
1,1-dimethylcyclopropane
E
isobutene
Conditions | Yield |
---|---|
With hydrogen In toluene High Pressure; 5 atm H2, room temp., complete reaction at 52°C for 2 h; GLC; | A 4% B 69% C 6% D 14% E 6% |
A
methane
B
ethane
C
2,2-dimethylpropane
D
1,1-dimethylcyclopropane
E
isobutene
Conditions | Yield |
---|---|
With hydrogen In toluene High Pressure; 5 atm H2, room temp., complete reaction at 52°C for 2 h; i-C4H8 and i-C5H12 also formed; GLC; | A 53% B 7% C 10% D 32% E 62% |
2,2,3,3-tetramethylcyclopropane
cis-hydrido(2,2,3,3-tetramethylcyclopropyl){bis(dicyclohexylphosphino)ethane}platinum(II)
cis-hydrido{(1,2,2-trimethylcyclopropyl)methyl}{bis(dicyclohexylphosphino)ethane}platinum(II)
C
2,2-dimethylpropane
Conditions | Yield |
---|---|
In further solvent(s) Kinetics; thermolysis of cis-hydridoneopentyl{bis(dicyclohexylphosphino)ethane}platinum(II) in 1,1,2,2-tetramethylcyclopropane via supposed {bis(dicyclohexylphosphino)ethane}platinum(0) at 35.0°C for 154 h; | A 56% B 12% C n/a |
In further solvent(s) Kinetics; thermolysis of cis-hydridoneopentyl{bis(dicyclohexylphosphino)ethane}platinum(II) in 1,1,2,2-tetramethylcyclopropane via supposed {bis(dicyclohexylphosphino)ethane}platinum(0) at 44.9°C for 28.5 h; | A 54% B 12% C n/a |
A
2,2-dimethylpropane
B
ethene
C
1,1-dimethylcyclopropane
D
3-Methyl-1-butene
E
isobutene
Conditions | Yield |
---|---|
With triphenylphosphine In toluene inert atmosphere, thermal decompn. (24°C, 5-fold molar excess PPh3); GLC; | A 2% B 28% C 11% D 7% E 52% |
In toluene inert atmosphere, thermal decompn. (24°C); GLC; | A 6% B 15% C 47% D 6% E 26% |
2,2-dimethylpropane
D-(-)-quinic acid
(1S,3R,4S,5R)-3,4-O-isopropylidene-1,5-quinic lactone
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In ethyl acetate at 0 - 78℃; for 12h; | 92% |
2,2-dimethylpropane
Conditions | Yield |
---|---|
With sulfuric acid In acetone at 20 - 45℃; for 1h; | 90% |
2,2-dimethylpropane
Conditions | Yield |
---|---|
With sulfuric acid In acetone at 20 - 45℃; for 1h; | 90% |
Conditions | Yield |
---|---|
With dichloromethane; antimony pentafluoride 1.) -78 deg C, 2 h, 2.) RT, 24 h; | 88% |
2,2-dimethylpropane
A
methane
B
ethane
C
propane
D
Isobutane
E
methylbutane
Conditions | Yield |
---|---|
With hydrogen; platinum at 243℃; Product distribution; further reaction temperatures, catalysts; | A 2.7% B 1.5% C 1.5% D 6.7% E 87.8% |
at 304℃; Product distribution; also from n-butane, other products,other temperatures, other catalysts; | A 7% B 1.7% C 2.4% D 15.6% E 73.3% |
With hydrogen; NaY-500; palladium at 216℃; Product distribution; Kinetics; Thermodynamic data; other catalysts, other temperatures; activation energies; | |
With hydrogen In neat (no solvent) at 275℃; under 1225.5 Torr; Reagent/catalyst; Inert atmosphere; |
pentamethylcyclopentadienyliridium(III) PMe3 dihydride
2,2-dimethylpropane
Conditions | Yield |
---|---|
In neat (no solvent) Irradiation (UV/VIS); dihydride Ir complex and C(CH3)4 irradiating for 5.3 h, cooling to -40°C, filtering, filtrate collecting, solvent removing in vacuo; identified by elem. anal., IR and NMR spectra; | 83% |
In further solvent(s) Irradiation (UV/VIS); irradn. in neopentane for 5.3 h; | 80% |
In further solvent(s) Irradiation (UV/VIS); soln. of complex in neopentane was irradiated for 36 h, then heated at 115°C for 21 h (inert atm.); cold chromy.(-80°C) on alumina III column, Et2O-hexane; elem. anal.; | 40% |
In neat (no solvent) Irradiation (UV/VIS); (1)H-, (13)C-NMR and IR spectroscopy; |
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