Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275844Generated: October 26, 2026

Methanol → 2-Amino-5-chloro-alpha-(2-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol

https://huagongshe.com/reaction/275844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Amino-2'-tert-butoxycarbonylaminomethyl-5-chlorobenzophenoneHCID 18315377—
SolventEthyl AcetateHCID 8857—
Product2-Amino-5-chloro-alpha-(2-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 5398938299.4%

Reaction Steps

To a methanol (5 ml) solution of 2-amino-2′-tert-butoxycarbonylaminomethyl-5-chlorobenzophenone (0.5 g) was added sodium borohydride (79 mg). The mixture was stirred for 3 hours at room temperature. To the reaction mixture was added acetic acid ethyl ester (100 ml), which was washed with water and, then, dried over anhydrous MgSO4. The solvent was distilled off, and the residue was purified by means of a silica gel column chromatography to give the object 2-amino-5-chloro-α-(2-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.5 g) as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352982B1
Source datasetuspto-grants-2002_03
ORD IDord-fb242133f4ca4d78ba15ec50d239e3ba
Source noteuspto-grants-2002_03