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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875170Generated: October 26, 2026

Sodium Acetate → 4'-hydroxymethyl-biphenyl-2-carbonitrile

https://huagongshe.com/reaction/875170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant4'-(Bromomethyl)-2-cyanobiphenylHCID 1501912—
ReactantHCID 178447302HCID 178447302—
SolventAcetic AcidHCID 176—
Product4'-hydroxymethyl-biphenyl-2-carbonitrileHCID 1393896—

Reaction Steps

According to U.S. Pat. No. 5,399,578, the process for the preparation of Valsartan (I) involves the reaction of 4′-bromomethyl-2-cyanobiphenyl (II) with sodium acetate and glacial acetic acid to produce 2′-cyano-4-hydroxymethylbiphenyl (III), which is reacted with oxalyl chloride in dichloromethane and dimethyl sulfoxide to produce 2′-cyano-4-formylbiphenyl (IV), which is further reacted with (L)-valine methyl ester hydrochloride (V) and sodium cyanoborohydride to produce N-[(2′-cyanobiphenyl-4-yl)methyl]-(L)-valine methyl ester (VI), followed by treatment with valeryl chloride to produce N-valeryl-N-[(2′-cyanobiphenyl-4-yl)methyl]-(L)-valine methyl ester (VII), which is treated with tri-n-butyltin azide followed by flash chromatography to produce Valsartan of formula (I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981109B2
Source datasetuspto-grants-2015_03
ORD IDord-61fab70841e14736a16695e43af93b77
Source noteuspto-grants-2015_03