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HRID 4318作成日:2026年10月24日

Hydrochloric Acid → 1,3-Bis[4-(3-chlorobenzyl)-1-piperazinyl]propane dihydrochloride monohydrate

https://huagongshe.com/ja/reaction/4318

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物1-(3-Chlorobenzyl)piperazineHCID 764727—
反応物Dichloromethane methanol ammonium hydroxideHCID 21896990—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TriethylamineHCID 8471—
生成物1,3-Bis[4-(3-chlorobenzyl)-1-piperazinyl]propane dihydrochloride monohydrateHCID 2015223968%

反応手順

A mixture of 6.3 g of 1-(3-chlorobenzyl)piperazine, 2.4 g of 1-bromo-3-chloropropane, 50 ml of reagent ethanol and 3.0 g of triethylamine was refluxed for 4 hours. Water (70 ml) was added, and the mixture was concentrated under vacuum to about 70 ml. The resulting aqueous mixture was extracted with ether (3×150 ml), and the extract was concentrated under vacuum to give a reddish-yellow oil. Chromatography of this oil on a silica column, the eluant being CH2Cl2 /CH3OH/ammonium hydroxide (45:5:1), resulted in an oil which was dissolved in 50 ml of ethanol. Hydrogen chloride-saturated ether was added to this solution until the mixture tested acidic to litmus. The resulting precipitate was filtered off, dried and weighed to yield 5.6 g (68% of theory) of 1,3-bis[4-(3-chlorobenzyl)-1-piperazinyl]propane dihydrochloride monohydrate. Recrystallization from water gave a white crystalline solid (m.p. 248°-257° C., with decomp.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725597
出典データセットuspto-grants-1988_02
ORD IDord-7341df2adb3541c79cb658048cb382de
出典メモuspto-grants-1988_02