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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295808Generated: October 30, 2026

HCID 178492988, compound → 5-Chloro-2-methoxy-4-(piperidin-1-yl)-phenylacetic acid

https://huagongshe.com/reaction/2295808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178492988HCID 178492988—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product5-Chloro-2-methoxy-4-(piperidin-1-yl)-phenylacetic acidHCID 54183470—

Reaction Steps

A solution of 11.07 g (30 mmoles) of 5-chloro-2-methoxy-4-(piperidin-1-yl)-phenylthioacetic acid morpholinamide in 120 ml of glacial acetic acid and 30 ml of concentrated hydrochloric acid is boiled under reflux for 22 hours. The reaction mixture is cooled, diluted with water and extracted with methylene chloride. The combined methylene chloride phases are washed with water, dried over sodium sulphate and concentrated by evaporation in a high vacuum rotary evaporator. Chromatography over silica gel with chloroform/methanol (19:1) yields 5-chloro-2-methoxy-4-(piperidin-1-yl)-phenylacetic acid which, after recrystallisation with methylene chloride/hexane, melts at 120°-122°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04426380
Source datasetuspto-grants-1984_01
ORD IDord-2228e9b80e94484a8b6fe1ef23a6c477
Source noteuspto-grants-1984_01