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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275853Generated: October 31, 2026

Methanol → 2-Amino-5-chloro-alpha-[4-(2-tert-butoxycarbonylaminoethyl)phenyl]benzyl alcohol

https://huagongshe.com/reaction/275853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Amino-4'-(2-tert-butoxycarbonylaminoethyl)-5-chlorobenzophenoneHCID 18315378—
SolventEthyl AcetateHCID 8857—
Product2-Amino-5-chloro-alpha-[4-(2-tert-butoxycarbonylaminoethyl)phenyl]benzyl alcoholHCID 69696774109.4%

Reaction Steps

To a methanol (40 ml) solution of 2-amino-4′-(2-tert-butoxycarbonylaminoethyl)-5-chlorobenzophenone (2.0 g) was added sodium borohydride (0.5 g). The mixture was stirred for 30 minutes at room temperature, to which was added acetic acid ethyl ester (100 ml). The mixture was washed with water and, then, dried over anhydrous MgSO4, followed by distilling off the solvent. The residue was purified by means of a silica gel column chromatography to give the object 2-amino-5-chloro-α-[4-(2-tert-butoxycarbonylaminoethyl)phenyl]benzyl alcohol (2.2 g) as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352982B1
Source datasetuspto-grants-2002_03
ORD IDord-3adf72da0be14c7887c69b66cc2df0cc
Source noteuspto-grants-2002_03