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2-AMINO-3-METHYLBENZYL ALCOHOL

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CAS:57772-50-6
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Products Intro: Product Name:2-amino-3-methylbenzyl alcohol
CAS:57772-50-6

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2-AMINO-3-METHYLBENZYL ALCOHOL Basic information
Product Name:2-AMINO-3-METHYLBENZYL ALCOHOL
Synonyms:(2-AMINO-3-METHYL-PHENYL)-METHANOL;2-AMINO-3-METHYLBENZYL ALCOHOL;2-AMino-3-Methylbenzyl alcohol 97%;Benzenemethanol, 2-amino-3-methyl-;2-AMINO-3-METHYLBENZYL ALCOHOL USP/EP/BP;2-Amino-3-methylbenzenemethanol
CAS:57772-50-6
MF:C8H11NO
MW:137.18
EINECS:
Product Categories:Amino Alcohols;Organic Building Blocks;Oxygen Compounds
Mol File:57772-50-6.mol
2-AMINO-3-METHYLBENZYL ALCOHOL Structure
2-AMINO-3-METHYLBENZYL ALCOHOL Chemical Properties
Melting point 67-69 °C (lit.)
Boiling point 135-145℃ (12 Torr)
density 1.126±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform (Slightly)
form Solid
pka14.48±0.10(Predicted)
color White to Off-White
InChIInChI=1S/C8H11NO/c1-6-3-2-4-7(5-10)8(6)9/h2-4,10H,5,9H2,1H3
InChIKeyFWTCWZZOKOBJIR-UHFFFAOYSA-N
SMILESC1(CO)=CC=CC(C)=C1N
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
2-AMINO-3-METHYLBENZYL ALCOHOL Usage And Synthesis
Uses2-Amino-3-methylbenzyl alcohol may be used in chemical synthesis.
Synthesis
3-Methylanthranilic acid

4389-45-1

2-AMINO-3-METHYLBENZYL ALCOHOL

57772-50-6

GENERAL PROCEDURE: A solution was prepared by dissolving 2-amino-3-methylbenzoic acid (8.5 mmol) in THF (24 mL) at room temperature. In a separate vessel, a suspension of lithium aluminum hydride (20.4 mmol) in THF (10 mL) was prepared. The benzoic acid solution was added dropwise to the lithium aluminum hydride suspension over a period of 20 minutes. After the dropwise addition, the reaction mixture continued to be stirred at room temperature for 3.5 hours. Upon completion of the reaction, the reaction mixture was cooled to 0 °C and quenched by slow addition of H2O (10 mL). Subsequently, the suspension was filtered through a diatomaceous earth plug and washed with EtOAc (100 mL). The organic phase was washed with brine (30 mL), dried over anhydrous MgSO4 and finally concentrated under vacuum to give 2-amino-3-methylbenzyl alcohol.

References[1] Chemical Communications, 2017, vol. 53, # 1, p. 216 - 219
[2] Organic Letters, 2017, vol. 19, # 12, p. 3219 - 3222
[3] Tetrahedron Letters, 2017, vol. 58, # 40, p. 3795 - 3799
[4] Journal of the American Chemical Society, 2014, vol. 136, # 24, p. 8729 - 8737
[5] Journal of the American Chemical Society, 2017, vol. 139, # 2, p. 655 - 662
2-AMINO-3-METHYLBENZYL ALCOHOL Preparation Products And Raw materials
Raw materials3-Methylanthranilic acid-->Lithium Aluminum Hydride-->Tetrahydrofuran
Preparation Products2,8-Dimethylquinoline-->4-METHYL-7,8,9,10-TETRAHYDROAZEPINO[2,1-B]QUINAZOLIN-12(6H)-ONE
Tag:2-AMINO-3-METHYLBENZYL ALCOHOL(57772-50-6) Related Product Information
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