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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860015Generated: November 1, 2026

Sodium borohydride → Methyl 4-[3-(hydroxymethyl)phenyl]benzoate

https://huagongshe.com/reaction/1860015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 4-(3-formylphenyl)benzoateHCID 4321386—
SolventEthanolHCID 702—
ProductMethyl 4-[3-(hydroxymethyl)phenyl]benzoateHCID 139238971.9%

Reaction Steps

Sodium borohydride (132 mg) was added to a solution of methyl 3′-formylbiphenyl-4-carboxylate (720 mg), which is the product of Reference example 14(a), in ethanol (50 ml) at ambient temperature. The mixture was stirred under an atmosphere of nitrogen for 50 minutes. The reaction mixture was quenched with 50% acetic acid and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water and the layers were separated. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was crystallized from diisopropyl ether to afford the desired compound (522 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528525B1
Source datasetuspto-grants-2003_03
ORD IDord-613ebbfcf39a474f9a3effd1a7a8d645
Source noteuspto-grants-2003_03