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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383089Generated: October 30, 2026

Sodium borohydride → [4-Hydroxymethyl-2-phenylbenzoyl]methionine methyl ester

https://huagongshe.com/reaction/383089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Formyl-2-phenylbenzoyl methionine methyl esterHCID 10571267—
SolventEthanolHCID 702—
Product[4-Hydroxymethyl-2-phenylbenzoyl]methionine methyl esterHCID 20622833—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the resultant compound from Example 16E in ethanol at 0° C. is added sodium borohydride (0.5 equivalent), and the reaction is stirred at 0° C. until TLC analysis shows the reaction to be complete. The reaction mixture is extracted with ether, which is washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue is then purified by column chromatography on silica gel to afford the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310095B1
Source datasetuspto-grants-2001_10
ORD IDord-92a4f16ffc784e6485e16c1fb57faecf
Source noteuspto-grants-2001_10