HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975345Generated: November 1, 2026
Chloroacetyl chloride → HCID 9807390, compound
https://huagongshe.com/reaction/1975345
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19099473 | HCID 19099473 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 9807390 | HCID 9807390 | — |
Reaction Steps
22 g of 1-{4-[N-(2-isopropyloxyethyl)amino]benzoyl}-4-[2-(4-chlorophenyl)ethyl]piperazine (Example 2) and 20.7 g of potash are introduced into 650 ml of toluene, and the mixture is kept at 45° for 15 minutes. At that temperature and with stirring, a solution of 7.1 g of chloroacetyl chloride in 30 ml of toluene is added dropwise. The mixture is stirred for 30 minutes at 45° and then stirring is continued at room temperature. The reaction solution is diluted with 500 ml of ethyl acetate and washed twice with 250 ml of water each time. The oil obtained after concentration by evaporation is chromatographed over silica gel and recrystallised in the form of the hydrochloride from acetone/ether, yielding 1-{4-[N-(2-isopropyloxyethyl)-N-chloroacetylamino]benzoyl}-4-[2-(4-chlorophenyl)ethyl]piperazine hydrochloride having a melting point of 146°-147°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05286728 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-5e481a0a04834e0f8d33f75559841784 |
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| Source note | uspto-grants-1994_02 |
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