Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534485Generated: October 30, 2026

2'-Aminoacetophenone → 2-Amino-alpha-methylbenzenemethanol

https://huagongshe.com/reaction/1534485

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-AminoacetophenoneHCID 11086—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product2-Amino-alpha-methylbenzenemethanolHCID 11205864%

Reaction Steps

Sodium borohydride (40 g, 1.0 mol) was added portion wise to a stirred solution of o-aminoacetophenone (80 g) in methanol (800 ml) at 0°, allowing the effervescence to subside between each addition. Cooling was removed and the mixture allowed to warm to reflux temperature to complete the reaction. When cool, the solvent was evaporated and the residue partioned between dichloromethane-water. The organic solution was washed successively with water and brine, dried (anhyd. MgSO4), filtered and evaporated to a light yellow oil which crystallized from petroleum spirit (40°-60°) to give white crystals (52 g, 64%), m.p. 50°-52°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089504
Source datasetuspto-grants-1992_02
ORD IDord-e09b0e34a6584703987db3800aaaedf7
Source noteuspto-grants-1992_02