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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649955Generated: October 31, 2026

Hydrochloric Acid → (4-Carboxymethoxyphenyl)-4-methoxyphenylcarbinol

https://huagongshe.com/reaction/1649955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(4-Methoxybenzoyl)phenoxyacetic acidHCID 14304542—
SolventMethanolHCID 887—
Solvent4-MethylmorpholineHCID 7972—
Product(4-Carboxymethoxyphenyl)-4-methoxyphenylcarbinolHCID 13966820—

Reaction Steps

11.2 g of 4-(4-methoxybenzoyl)phenoxyacetic acid are dissolved in 600 ml of 80% strength methanol (reflux), and 4.4 ml of N-methylmorpholine are added. 6 g of sodium borohydride are added in portions over the course of two hours, and the reaction is continued under reflux conditions for 3 hours. The mixture is cooled to room temperature and acidified to pH 2.5 with 3N HCl. The methanol is distilled off, the aqueous phase is extracted with ethyl acetate, and the organic phase is washed with brine and dried over sodium sulfate. After removal of the ethyl acetate by distillation there remains a white amorphous powder. The product is used directly for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04922015
Source datasetuspto-grants-1990_05
ORD IDord-8bed4e1881904129ba0bbf6e1c56e831
Source noteuspto-grants-1990_05