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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | o-Methoxycarbonyl--[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide | HCID 13117363 | — |
| Reactant | Potassium hydroxide methanol | HCID 23689386 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | o-Carboxy--[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide monohydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04585774 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-50fe267d546d4303a5f4e55d8ef24b8b |
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| Source note | uspto-grants-1986_04 |
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