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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082577Generated: November 4, 2026

Hydrochloric Acid → N-(ethoxycarbonylmethyl)-2-(4-hydroxymethylphenoxy)acetamide

https://huagongshe.com/reaction/2082577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantN-(ethoxycarbonylmethyl)-2-(4-formylphenoxy)acetamideHCID 21848352—
SolventEthanolHCID 702—
ProductN-(ethoxycarbonylmethyl)-2-(4-hydroxymethylphenoxy)acetamideHCID 2184838986.9%

Reaction Steps

To a mixture of N-(ethoxycarbonylmethyl)-2-(4-formylphenoxy)acetamide (4.6 g) and ethanol (150 ml) was added under ice cooling sodium borohydride (0.25 g), and the mixture was stirred at room temperature for 30 minutes. To the reaction mixture was added 3% hydrochloric acid, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure gave N-(ethoxycarbonylmethyl)-2-(4-hydroxymethylphenoxy)acetamide (4.03 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05189211
Source datasetuspto-grants-1993_02
ORD IDord-1804c0c139214dfba2088e34716bccc5
Source noteuspto-grants-1993_02