HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290473Generated: November 1, 2026
Potassium Carbonate → n-Butyl 3-{4-[1-(4-chlorophenyl)-piperazin-4-yl]-phenyl}-propionate
https://huagongshe.com/reaction/2290473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-N,N-bis(2-chloroethyl)aniline | HCID 95112 | — |
| Reactant | n-Butyl 3-(4-aminophenyl)-propionate | HCID 20232483 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | n-Butyl 3-{4-[1-(4-chlorophenyl)-piperazin-4-yl]-phenyl}-propionate | HCID 20232689 | — |
Reaction Steps
A mixture of 12.3 g. (55 mmole) n-butyl 3-(4-aminophenyl)-propionate, 16.0 g. (55 mmole) N,N-bis-(2-chloroethyl)-4-chloroaniline and 50 ml. n-butanol is maintained at reflux temperature for 48 hours, then 3.8 g. (27 mmole) pulverised anhydrous potassium carbonate are added thereto and stirring continued for 1 week at reflux temperature. Thereafter, it is suction filtered hot, the filtrate is evaporated in a vacuum and the residue is stirred with ligroin and suction filtered. The product is now taken up in diethyl ether, filtered and mixed with hydrogen chloride-containing diethyl ether. Since the hydrochloride is difficult to suction filter, the ether phase is evaporated in a vacuum and the residue recrystallised from n-butanol. Yield 9.5 g. (39% of theory) of hydrochloride; m.p. 179°-183° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04616086 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-79b09a8cbda04c408288e3347f25ef64 |
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| Source note | uspto-grants-1986_10 |
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