HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290458Generated: October 30, 2026
(3-Bromopropyl)benzene → HCID 11989461, compound
https://huagongshe.com/reaction/2290458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | Ethyl 4-[2-(1-piperazinyl)ethyl]benzoate | HCID 20232457 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 11989461 | HCID 11989461 | 76% |
Reaction Steps
A mixture of 40 ml. HMPT, 23.6 g. (90 mmole) ethyl 4-[2-(piperazin-1-yl)-ethyl]-benzoate and 8.96 g. (45 mmole) 3-bromopropylbenzene is maintained at 110° C. for 22 hours, whereby, immediately after mixing together, the temperature increases to about 55° C. and the formation of a pale precipitate is observed. At 110° C., a clear, red-brown solution is present, from which, upon cooling, a product crystallises out. It is poured into a little water, extracted with diethyl ether, the ether phase is washed with water, dried with anhydrous sodium sulphate and evaporated. The crude product is dissolved in diethyl ether and converted into the dihydrochloride by means of hydrogen chloride-containing diethyl ether and recrystallised from ethanol containing 2 drops of concentrated hydrochloric acid; m.p. 273° C. (decomp.). Yield 76% of theory.
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-2d56195009c14de8ac7cb3f36f5c09dc |
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| Source note | uspto-grants-1986_10 |
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