HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381187Generated: November 2, 2026
Chloroacetic Acid → [4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-acetic acid
https://huagongshe.com/reaction/1381187
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetic Acid | HCID 300 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(3,4-Dimethoxybenzoyl)piperazine | HCID 873407 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-acetic acid | HCID 20235788 | — |
Reaction Steps
32 Grams of 4-(3,4-dimethoxybenzoyl)piperazine and 13.1 g of potassium hydroxide were dissolved in 300 ml of dimethylformamide (DMF), then under an ice-cooled condition with stirring, 10 g of α-chloroacetic acid was added thereto, next the reaction mixture was heated at 50° C. for 5 hours with stirring. After completion of the reaction, the reaction mixture was concentrated to dryness, the residue obtained was dissolved in water. The solution obtained was washed with chloroform, the aqueous layer was neutralized with concentrated hydrochloric acid, crystals formed were collected by filtration to obtain 9.8 g of α-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetic acid.
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-cb775512a34841e3a8513111fa5f2c5b |
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| Source note | uspto-grants-1986_04 |
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