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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762865Generated: October 30, 2026

4-Aminophenol → HCID 14500502, compound

https://huagongshe.com/reaction/1762865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
Reactant4-Bromobutyryl chlorideHCID 70225—
SolventAcetoneHCID 180—
ProductHCID 14500502HCID 1450050252%

Reaction Steps

A mixture of 30.9 g (0.28 mol) of p-aminophenol in about 300 mL of acetone was stirred in an ice bath and a solution of 25 g (0.14 mol) of 4-bromobutyryl chloride in about 50 mL of acetone was dripped in over 20 minutes. The reaction was stirred cold for another 1/2 hour and then at room temperature for two hours. It was then ice cooled and the mixture filtered. The precipitate was washed with about 200 mL of cold acetone. The filtrate was evaporated and the residue slurried in about 200 mL of 1N HCl, whereupon a precipitate formed. The mixture was ice cooled, filtered, and the precipitate was washed with additional 1N HCl followed by water. The precipitate was dissolved in about 100 mL of ethanol at room temperature, diluted with about 160 mL of water, ice cooled and filtered. The precipitate was washed with a mixture of water and ethanol and then with hexane to yield 18.1 g (52%) of 4-bromo-N-(4-hydroxyphenyl)butanamide, mp 142.5°-144.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835180
Source datasetuspto-grants-1989_05
ORD IDord-4aff0509a12b491fbe0b8f9a60f1bbc3
Source noteuspto-grants-1989_05