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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758220Generated: November 4, 2026

Hydrochloric Acid → 4-Amino-alpha-methylbenzenemethanol

https://huagongshe.com/reaction/1758220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-NitroacetophenoneHCID 7487—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product4-Amino-alpha-methylbenzenemethanolHCID 8575379%

Reaction Steps

Under nitrogen, 2.85 g (75 mmol) sodium borohydride, 500 mg (0.9 mmol) cobalt (II) phthalocyanine and 1.65 g (10 mmol) p-nitro acetophenone are agitated in 50 ml ethanol for 48 hours at 20° C. The reaction mixture is acidified with 5N hydrochloric acid, cooling with ice, and the blue precipitate is centrifuged which is washed with methanol. The centrifugate collected is concentrated and the residue separated into water and ether. The water phase is alkalized with sodium hydroxide and extraction is accomplished with ether. The ether phase is dried with sodium sulfate and concentrated, leaving behind 1.08 g (79%) α-(p-aminophenyl)-ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04372893
Source datasetuspto-grants-1983_02
ORD IDord-0eb3f51cb7ca41d484795720b517e143
Source noteuspto-grants-1983_02