lithium aluminium tetrahydride
1-hexene
di(n-hexyl)aluminum chloride
trihexylaluminium
Conditions | Yield |
---|---|
In n-heptane byproducts: LiCl; LiAlH4 loaded in a vertical-type ball mill under Ar or N2; heptane added; mixt. agitated for 15 min at 70°C; mixt. of (C6H13)2AlCl with hex-1-ene (LiAlH4:(C6H13)2AlCl:hex-1-ene=1.1:1.0:4.5) added; mixt. agitated for 1.5 h at 90°C; cooled; filtered under Ar; solvent and olefin removed (vac., 10 Torr) at60-70°C; elem. anal.; | 95% |
Conditions | Yield |
---|---|
With triisobutylaluminum In hexane (N2); heating (autoclave, 140°C, 1 h, 120°C, 8 h); distn.; elem. anal.; | 89.1% |
With NaAlEt4 In toluene under N2 or Ar; mixt. of AlH3, NaAlEt4, olefin (3.8 equiv.) and toluene heated at reflux; after 20 min temp. raised from 80 to 100°C and gradually decreased to 70-80°C; 2 h; cooled; filtered; ppt. washed with hexane; solvent and excess olefin removed in vac. at 60-80°C (7 Torr); elem. anal.; |
Conditions | Yield |
---|---|
Stage #1: 3-hexene; tri-n-propylaluminum at 70℃; under 760.051 Torr; Heating / reflux; Stage #2: cobalt(III) acetylacetonate In toluene for 2h; Stage #3: With hydrogenchloride | 6.1% |
Conditions | Yield |
---|---|
With aluminium hydride | |
With lithium aluminium tetrahydride |
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane for 1h; Product distribution; Ambient temperature; other reaction time; other reagent: ZnCl2; other molecular proportion.; | 90% |
With aluminium trichloride In dichloromethane for 1h; Ambient temperature; | 90% |
Conditions | Yield |
---|---|
With iron(III) chloride In various solvent(s) at 40℃; for 15h; | A 86% B n/a |
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane for 1h; Product distribution; Ambient temperature; other molecular proportion.; | 84% |
With aluminium trichloride In dichloromethane for 1h; Ambient temperature; | 84% |
Conditions | Yield |
---|---|
In toluene at -5 - 50℃; for 7h; Inert atmosphere; | 81.8% |
In toluene at -5 - 50℃; for 7h; Inert atmosphere; | 81.8% |
Conditions | Yield |
---|---|
With dilithium tetrachlorocuprate; triphenylphosphine In octane at 50℃; for 5h; | 78% |
Conditions | Yield |
---|---|
Stage #1: 1-hexene; trihexylaluminium With zirconocene dichloride In hexane at 0 - 20℃; Stage #2: butyraldehyde With copper(l) chloride In hexane at -15 - 20℃; | 78% |
Conditions | Yield |
---|---|
Stage #1: N,N'-ethylenediphthalimide; trihexylaluminium In toluene at -5 - 50℃; for 8h; Inert atmosphere; Stage #2: With water In toluene at 20℃; Inert atmosphere; | 78% |
Conditions | Yield |
---|---|
Stage #1: 1-hexene; trihexylaluminium With zirconocene dichloride In hexane at 0 - 20℃; Stage #2: isobutyraldehyde With copper(l) chloride In hexane at -15 - 20℃; | 76% |
Conditions | Yield |
---|---|
bis-triphenylphosphine-palladium(II) chloride In diethyl ether for 4h; Heating; | 75% |
trihexylaluminium
Conditions | Yield |
---|---|
Stage #1: N-benzyl-N-(3-oxobutyl)-(E)-3-phenylpropenamide With bis-acetylacetonatocobalt(II) dihydrate In tetrahydrofuran at 0 - 20℃; for 0.5h; Stage #2: trihexylaluminium In tetrahydrofuran; hexane at 0 - 20℃; for 15h; diastereoselective reaction; | 75% |
Conditions | Yield |
---|---|
In toluene at -5 - 80℃; for 2h; Inert atmosphere; | 75% |
In toluene at -5 - 80℃; for 2h; Inert atmosphere; | 75% |
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane | 70% |
(1R,2R)-trans-N-phthaloyl-1,2-diaminocyclohexane
trihexylaluminium
Conditions | Yield |
---|---|
In hexane at -5 - 40℃; for 2h; Inert atmosphere; | 69.8% |
In hexane at -5 - 40℃; for 2h; Inert atmosphere; | 69.8% |
Conditions | Yield |
---|---|
In toluene at -5 - 90℃; for 2h; Inert atmosphere; | 69.1% |
In toluene at -5 - 90℃; for 2h; Inert atmosphere; | 69.1% |
In toluene at -5 - 90℃; for 2h; Inert atmosphere; | 69.1% |
Conditions | Yield |
---|---|
With iron(III) chloride In hexane at 25℃; | 67% |
trihexylaluminium
dimethyl 2-phenyl-cycloprop-2-ene-1,1-dicarboxylic ester
dimethyl (E)-2-(2-phenyloct-1-enyl)malonate
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate In tetrahydrofuran; hexane at 0 - 20℃; for 16h; stereoselective reaction; | 66% |
chloro-trimethyl-silane
trihexylaluminium
A
trimethylhexylsilane
B
di-n-hexyldimethylsilane
Conditions | Yield |
---|---|
With potassium chloride at 150℃; for 6h; | A 65% B 35% |
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane -10 deg C, then 20 deg C, 1 h; | 65% |
rac-3-acetoxycyclohexene
trihexylaluminium
Conditions | Yield |
---|---|
With copper(I) bromide In hexane at 25℃; | 63% |
Conditions | Yield |
---|---|
In dichloromethane | 62% |
acetic acid-(1,1-dimethyl-pent-4-en-2-ynyl ester)
trihexylaluminium
2-methyl-4-hexyl-2,3,5-hexatriene
Conditions | Yield |
---|---|
iron(III) chloride In diethyl ether at 20℃; for 2h; | 62% |
acetic acid-(1,1-dimethyl-pent-4-en-2-ynyl ester)
trihexylaluminium
A
2-methyl-4-hexyl-2,3,5-hexatriene
Conditions | Yield |
---|---|
With iron(III) chloride In diethyl ether at 20℃; for 2h; | A 62% B n/a |
N-benzyl-N-(3-oxobutyl)-(E)-3-(4-methoxyphenyl)propenamide
trihexylaluminium
Conditions | Yield |
---|---|
Stage #1: N-benzyl-N-(3-oxobutyl)-(E)-3-(4-methoxyphenyl)propenamide With bis-acetylacetonatocobalt(II) dihydrate In tetrahydrofuran at 0 - 20℃; for 18h; Stage #2: trihexylaluminium In tetrahydrofuran; hexane at 0 - 20℃; for 23h; diastereoselective reaction; | 61% |
trihexylaluminium
dimethylsilicon dichloride
A
dimethylhexylsilyl chloride
B
di-n-hexyldimethylsilane
C
dimethylhexylsilane
Conditions | Yield |
---|---|
With potassium chloride at 150℃; for 3h; | A 31% B 58% C 11% |
With potassium chloride at 150℃; for 3h; | A 56% B 34% C 10% |
2-butylcycloprop-2-ene-1,1-dicarboxylic acid dimethyl ester
trihexylaluminium
dimethyl (Z)-2-(2-butyloct-1-enyl)malonate
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate In tetrahydrofuran; hexane at 0 - 20℃; for 16h; stereoselective reaction; | 52% |
trans-(Mo6Cl8)Cl4(tributylphosphine)2
trihexylaluminium
all-trans-(Mo6Cl8)Cl2(n-C6H13)2(tributylphosphine)2
Conditions | Yield |
---|---|
In toluene (N2); a soln. of Al(C6H13)3 added to a suspn. of Mo-compound at -15°C; stirred at -15°C for 20 h; evapd. in vacuo; ether added; ppte. washed with ether; dried in vacuo; dissolved in toluene at 60°C; filtered; concentrated; cooled to -20°C; elem. anal.; | 8% |
Molecular structure of Tri-n-hexylaluminium (CAS NO.1116-73-0) is:
Product Name: Tri-n-hexylaluminium
CAS Registry Number: 1116-73-0
IUPAC Name: Trihexylalumane
Molecular Weight: 282.483798 [g/mol]
Molecular Formula: C18H39Al
H-Bond Donor: 0
H-Bond Acceptor: 0
EINECS: 214-241-6
Density: 0.686 g/cm3
Storage temp.: Flammables + water-Freezer (-20 °C)e area
Product Categories: Organometallics
Canonical SMILES: CCCCCC[Al](CCCCCC)CCCCCC
InChI: InChI=1S/3C6H13.Al/c3*1-3-5-6-4-2;/h3*1,3-6H2,2H3;
InChIKey: ORYGRKHDLWYTKX-UHFFFAOYSA-N
Safty information about Tri-n-hexylaluminium (CAS NO.1116-73-0) is:
Hazard Codes: N; C; F
Risk Statements: 67-65-62-51/53-48/20-34-14/15-11
R67:Vapours may cause drowsiness and dizziness.
R65:Harmful: may cause lung damage if swallowed.
R62:Risk of impaired fertility.
R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
R48/20:Danger of serious damage to health by prolonged exposure and harmful by inhalation.
R34:Causes burns.
R14/15 :Reacts violently with water and contact with water liberates extremely flammable gases.
R11:Highly flammable.
Safety Statements: 6A-61-45-43B-36/37/39-24/25-16
S6:Keep under ... (there follows the name of an inert gas).
S61:Avoid release to the environment. Refer to special instructions / safety data sheets.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S43:In case of fire use ... (there follows the type of fire-fighting equipment to be used.)
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
S24/25:Avoid contact with skin and eyes.
S16:Keep away from sources of ignition.
RIDADR: 3051
HazardClass: 4.2
PackingGroup: I
Tri-n-hexylaluminium , its cas register number is 1116-73-0. It also can be called Trihexylalane ; Aluminum, trihexyl- ; Trihexylaluminium .It is a clear colorless solution.
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