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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38685Generated: October 26, 2026

Sodium borohydride → (2'-Hydroxymethyl-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/38685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(2'-Formyl-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl esterHCID 86633171—
SolventMethanolHCID 887—
Product(2'-Hydroxymethyl-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl esterHCID 67431174—

Reaction Steps

To (2′-formyl-6-methoxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl ester (0.844 g, 2.30 mmol) in MeOH was added sodium borohydride (0.096 g, 2.53 mmol), and the reaction was stirred at room temperature for 15 minutes. The mixture was concentrated, and the residue was partitioned between EtOAc and H2O. The aqueous layer was extracted with EtOAc, and the combined organic layers were dried over MgSO4, filtered, and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524748B2
Source datasetuspto-grants-2013_09
ORD IDord-b42e430b52dd4fcbb22ed453d0a0b178
Source noteuspto-grants-2013_09