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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4'-(Bromomethyl)-2-cyanobiphenyl | HCID 1501912 | — |
| Reactant | HCID 178447302 | HCID 178447302 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4'-hydroxymethyl-biphenyl-2-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08981109B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-61fab70841e14736a16695e43af93b77 |
|---|
| Source note | uspto-grants-2015_03 |
|---|