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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413955Generated: November 4, 2026

3-Chloro-4-fluoroaniline → HCID 14076517, compound

https://huagongshe.com/reaction/2413955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-fluoroanilineHCID 9708—
Reactantbeta-BUTYROLACTONEHCID 18303—
SolventDiethyl EtherHCID 3283—
ProductHCID 14076517HCID 1407651747.9%

Reaction Steps

86 g (1.00 mole) of β-butyrolactone was added to 146 g (1.00 mole) of 3-chloro-4-fluoroaniline, and this mixture was stirred at 80°-90° C. for 30 minutes and then allowed to cool to room temperature. To the resulting reaction solution was added 1000 ml of ether. This mixture was filtered to remove any insoluble matter, and the filtrate thus obtained was extracted with 750 ml of a 2N aqueous solution of sodium hydroxide. This extract was acidified with 130 ml of concentrated hydrochloric acid and then extracted with 1000 ml of ether. The ether layer was separated, dried over anhydrous sodium sulfate and then evaporated to dryness. Thus, there was obtained 111 g (47.9% yield) of 3-(3-chloro-4-fluoro-anilino) butyric acid in the form of pale-yellow oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04720495
Source datasetuspto-grants-1988_01
ORD IDord-ecf1d1918ee84b1da5d227ccc3a84722
Source noteuspto-grants-1988_01