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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381202Generated: October 31, 2026

Hydrochloric Acid → o-Carboxy--[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide monohydrochloride

https://huagongshe.com/reaction/1381202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactanto-Methoxycarbonyl--[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilideHCID 13117363—
ReactantPotassium hydroxide methanolHCID 23689386—
SolventEthanolHCID 702—
Producto-Carboxy--[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide monohydrochlorideHCID 23323535—

Reaction Steps

20 Grams of o-methoxycarbonyl- -[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide, 400 ml of methanol and 25 ml of 3.5N-potassium hydroxide methanol solution were mixed together and the mixture was refluxed for 8.5 hours. After completion of the reaction, the reaction mixture was allowed to stand for cooling, then an ethanol solution of hydrochloric acid was added to the mixture to adjust the pH thereof to about 1. The crystals formed were removed by filtration, and the mother liquor was cooled by ice. The crystals were collected by filtration, recrystallized from 80% water-containing methanol to obtain 13.28 g of o-carboxy- -[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide monohydrochloride in the form of colorless cotton fiber-like crystals. Melting point: 250.5°-251.5° C. (decomposed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585774
Source datasetuspto-grants-1986_04
ORD IDord-50fe267d546d4303a5f4e55d8ef24b8b
Source noteuspto-grants-1986_04