2-ethylbenzaldehyde
(2-ethylphenyl)methanol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol for 4h; Reduction; Heating; | 99% |
With sodium tetrahydroborate In ethanol at 0 - 25℃; for 2h; | 74% |
With sodium tetrahydroborate In methanol Heating; |
Conditions | Yield |
---|---|
With diborane In tetrahydrofuran at 0 - 20℃; for 24h; | 87% |
With diborane In tetrahydrofuran; methanol at 0 - 20℃; for 24h; | 87% |
Stage #1: 2-ethylbenzoic acid With boron trifluoride diethyl etherate In tetrahydrofuran at 0 - 20℃; for 24h; Stage #2: With methanol In tetrahydrofuran for 0.75h; | 87% |
2-ethynylbenzyl alcohol
(2-ethylphenyl)methanol
Conditions | Yield |
---|---|
With hydrogen In glycerol at 100℃; under 2250.23 Torr; for 24h; chemoselective reaction; | 84% |
2-acetyl-benzoic acid
A
3-methylphthalide
B
1-(1-hydroxyethyl)-2-hydroxymethylbenzene
C
(2-ethylphenyl)methanol
Conditions | Yield |
---|---|
With samarium diiodide; water In tetrahydrofuran for 0.0333333h; Ambient temperature; | A 41% B 36% C 11% |
Conditions | Yield |
---|---|
Stage #1: 2-methyl-benzyl alcohol With n-butyllithium In diethyl ether; hexane for 4h; Heating; Stage #2: methyl iodide In diethyl ether; hexane at 20℃; for 1h; | 33% |
Conditions | Yield |
---|---|
With diethyl ether |
ethanol
N-benzyl-N-nitrosobenzamide
A
benzoic acid benzyl ester
B
N-benzylbenzamide
C
(2-ethylphenyl)methanol
D
benzoic acid
Conditions | Yield |
---|---|
weitere Produkten: Benzylamin,Aethylnitrit,salpetrige Saeure; |
sodium phenoxide
benzyl potassium
ethyl ester of p-toluenesulfonic acid
A
(2-ethylphenyl)methanol
B
Phenetole
formaldehyd
ethylbenzene
A
(RS)-2-phenyl-1-propanol
B
(2-ethylphenyl)methanol
Conditions | Yield |
---|---|
multistep reaction; optional ortho and alpha hydroxymethylation of alkylarenes; | |
Yield given. Multistep reaction. Yields of byproduct given; |
2-ethylbenzoyl chloride
(2-ethylphenyl)methanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
Conditions | Yield |
---|---|
With naphthalene; lithium 1.) THF, 0 deg C, 2 h, 2.) THF, -10 deg C, 60 min; Yield given. Multistep reaction; | |
With naphthalene; lithium 1) THF, 0 deg C, 1.5 h, 2) THF, 0 deg C, 60 min; Yield given. Multistep reaction; |
1,3-dihydro-1-methylisobenzofuran
A
1-O-tolyl-ethanol
B
(2-ethylphenyl)methanol
Conditions | Yield |
---|---|
With naphthalene; water; lithium 1) THF, 0 deg C, 3 h; Yield given. Multistep reaction. Yields of byproduct given; |
benzyl chloride
A
Benzyl acetate
B
(2-ethylphenyl)methanol
C
benzyl alcohol
Conditions | Yield |
---|---|
bei der elektrolytischen Reduktion; |
Conditions | Yield |
---|---|
nachfolgend Zersetzung; |
Conditions | Yield |
---|---|
at 180℃; |
ethanol
N,N,N-tribenzyl methylammonium iodide
A
N-methyldibenzylamine
B
(2-ethylphenyl)methanol
ethanol
allyl-dibenzyl-methyl-ammonium; iodide
A
(2-ethylphenyl)methanol
B
N-allyl-N-α-methylbenzylamine
ethanol
benzyldimethylphenylammonium chloride
A
(2-ethylphenyl)methanol
B
N,N-dimethyl-aniline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1) sec-BuLi / 1) THF, -40 deg C, 2 h, 2) THF, 1 h 2: 1) Li, naphthalene, 2) H2O / 1) THF, 0 deg C, 3 h View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: NaBH4 / methanol / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) magnesium / 1.) ether 2: LiAlH4 / diethyl ether View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 16.8 percent / SnCl4 / CHCl3 View Scheme |
Conditions | Yield |
---|---|
With Cellulosimicrobium cellulans EB-8-4 at 30℃; for 10h; pH=7; Microbiological reaction; K-buffer containing glucose; Enzymatic reaction; regioselective reaction; | 94 %Chromat. |
N,N-diisopropylcarbamoyl chloride
(2-ethylphenyl)methanol
2-ethylbenzyl N,N-diisopropylcarbamate
Conditions | Yield |
---|---|
Stage #1: (2-ethylphenyl)methanol With sodium hydride In tetrahydrofuran; mineral oil at 0℃; Inert atmosphere; Stage #2: N,N-diisopropylcarbamoyl chloride In tetrahydrofuran; mineral oil at 20℃; for 48h; Inert atmosphere; | 98% |
(2-ethylphenyl)methanol
1-(bromomethyl)-2-ethylbenzene
Conditions | Yield |
---|---|
With phosphorus tribromide In diethyl ether at 20℃; for 0.166667h; | 94% |
With bromine; triphenylphosphine In dichloromethane Bromination; Heating; | 80% |
With hydrogen bromide |
Conditions | Yield |
---|---|
Stage #1: (2-ethylphenyl)methanol With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.5h; Stage #2: allyl bromide In tetrahydrofuran; mineral oil at 0 - 20℃; | 90% |
Conditions | Yield |
---|---|
With pyridine at 0℃; for 1.5h; | 89% |
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; copper(II) acetate monohydrate In water; dimethyl sulfoxide at 100 - 110℃; for 20h; Sealed tube; | 68% |
Conditions | Yield |
---|---|
With oxygen; eosin y In acetonitrile at 20℃; Irradiation; | 65% |
(Z)-1-bromo-2-(triisopropylsilyloxymethyl)but-2-ene
(2-ethylphenyl)methanol
(E)-1-(2-ethylbenzyloxy)-2-(triisopropylsilyloxymethyl)but-2-ene
Conditions | Yield |
---|---|
With potassium tert-butylate In tetrahydrofuran at 20℃; for 16h; | 63% |
4-amino-2-methylpyrimidine-5-carbaldehyde
(2-ethylphenyl)methanol
2-Methyl-6-(2-trifluoromethyl-phenyl)-pyrido[2,3-d]pyrimidin-7-ylamine
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol for 4h; Heating; | 45% |
(2-ethylphenyl)methanol
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In dichloromethane at 25℃; | 30% |
Conditions | Yield |
---|---|
With phosphorus pentoxide |
Conditions | Yield |
---|---|
at 160 - 180℃; |
Conditions | Yield |
---|---|
With phosphorus pentaoxide |
Conditions | Yield |
---|---|
With sodium at 130 - 210℃; |
(2-ethylphenyl)methanol
2-ethylbenzaldehyde
Conditions | Yield |
---|---|
With chromium(III) oxide; sulfuric acid | |
With chromium(VI) oxide; silica gel In diethyl ether; dichloromethane for 24h; | |
With dipyridinium dichromate; trichloroacetic acid In acetonitrile at 19.99℃; Kinetics; Further Variations:; Temperatures; |
Conditions | Yield |
---|---|
With iodine; chlorine |
Conditions | Yield |
---|---|
With thionyl chloride; N,N-diethylaniline | |
With thionyl chloride | |
With thionyl chloride In benzene Heating; | |
With thionyl chloride In benzene |
Conditions | Yield |
---|---|
With potassium acetate |
Conditions | Yield |
---|---|
With tin(IV) chloride | |
With phosphorus pentoxide |
Conditions | Yield |
---|---|
With titanium tetrachloride | |
With aluminium trichloride |
Conditions | Yield |
---|---|
With aluminium trichloride |
This chemical is called (2-Ethylphenyl)methanol, and it can also be named as 2-Ethylbenzyl alcohol. With the molecular formula of C9H12O, its product categories are Alcohols; C9 to C30; Oxygen Compounds. The CAS registry number of this chemical is 767-90-8. In addition, this chemical should be sealed in the ventilated and dry place, away from light.
Other characteristics of the (2-Ethylphenyl)methanol can be summarised as followings: (1)ACD/LogP: 2.03; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.03; (4)ACD/LogD (pH 7.4): 2.03; (5)ACD/BCF (pH 5.5): 20.41; (6)ACD/BCF (pH 7.4): 20.41; (7)ACD/KOC (pH 5.5): 301.4; (8)ACD/KOC (pH 7.4): 301.4; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 9.23 Å2; (13)Index of Refraction: 1.533; (14)Molar Refractivity: 42.25 cm3; (15)Molar Volume: 136 cm3; (16)Polarizability: 16.75×10-24cm3; (17)Surface Tension: 37.8 dyne/cm; (18)Density: 1 g/cm3; (19)Flash Point: 106.1 °C; (20)Enthalpy of Vaporization: 49.24 kJ/mol; (21)Boiling Point: 229.3 °C at 760 mmHg; (22)Vapour Pressure: 0.0393 mmHg at 25°C.
You can still convert the following datas into molecular structure:
1.SMILES: OCc1ccccc1CC
2.InChI: InChI=1/C9H12O/c1-2-8-5-3-4-6-9(8)7-10/h3-6,10H,2,7H2,1H3
3.InChIKey: SBUIQTMDIOLKAL-UHFFFAOYAQ
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