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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808Generated: October 26, 2026

Sodium borohydride → 2-Amino-alpha-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcohol

https://huagongshe.com/reaction/1808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Amino-4'-benzyloxy-5-chloro-2'-methoxybenzophenoneHCID 54005446—
SolventMethanolHCID 887—
Product2-Amino-alpha-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcoholHCID 5393195894.5%

Reaction Steps

To a solution of 2-amino-4'-benzyloxy-5-chloro-2'-methoxybenzophenone (10 g) in methanol (100 ml) was added sodium borohydride (1.4 g). After being stirred for 24 h, the mixture was concentrated in vacuo. The residue was diluted with water (200 ml) and extracted with ethyl acetate (300 ml). The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1-2:1) to give 2-amino-α-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcohol (9.5 g) as colorless crystals (mp=101°-103° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726306
Source datasetuspto-grants-1998_03
ORD IDord-8a08d4d95931403fb13cf9932fe3b98e
Source noteuspto-grants-1998_03