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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072149Generated: October 30, 2026

Ethanol → trans-N-(1,2,3,4-tetrahydro-4-hydroxy-1-naphthyl)acetamide

https://huagongshe.com/reaction/2072149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
ReactantN-(4-Oxo-1,2,3,4-tetrahydronaphthalen-1-yl)acetamideHCID 13037024—
SolventWaterHCID 962—
Producttrans-N-(1,2,3,4-tetrahydro-4-hydroxy-1-naphthyl)acetamideHCID 70619274—

Reaction Steps

A mixture of 19.2 g. of N-(1,2,3,4-tetrahydro-4-oxo-1-naphthyl)acetamide and 275 ml. of absolute ethanol is stirred under a nitrogen atmosphere and 3.58 g. sodium borohydride added. The reaction mixture is stirred at room temperature for 16 hours, then 200 ml. of water is added and the stirring continued for 4 hours. Next, the reaction mixture is evaporated to dryness in vacuo and the residue treated with 250 ml. of water. The mixture is cooled in an ice bath and acidified with concentrated hydrochloric acid. The precipitated yellow solid is collected and dried; weight 6 g., m.p. 120°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049717
Source datasetuspto-grants-1977_09
ORD IDord-ad9663ffbb4b4764a34ae45b0cf9b3e5
Source noteuspto-grants-1977_09