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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2290864생성일: 2026년 10월 27일

Dimethyl Sulfoxide → 1-(4-Methylbenzyl)-4-(3-chloropropyl)piperazine dihydrochloride

https://huagongshe.com/reaction/2290864

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물1-Bromo-3-chloropropaneHCID 8006—
반응물Potassium HydroxideHCID 14797—
반응물1-(4-Methylbenzyl)piperazineHCID 764723—
용매WaterHCID 962—
생성물1-(4-Methylbenzyl)-4-(3-chloropropyl)piperazine dihydrochlorideHCID 20153192274.5%

반응 단계

A mixture of 14.0 g of 1-(4-methylbenzyl)piperazine, 8.0 g of potassium hydroxide and 125 ml of dimethyl sulfoxide was stirred for 45 minutes. 11.8 g of 1-bromo-3-chloropropane were then added, and the mixture was stirred for an additional hour. Water was added, and the product was extracted with ether, and the extract was dried (sodium sulfate) and treated with ethereal hydrochloric acid to give 23.3 g (94% of theory) of 1-(4-methylbenzyl)-4-(3-chloropropyl)piperazine dihydrochloride as a white crystalline solid. (b) The procedure described in Example 1(b) was followed, using 7.7 g of thiourea, 23.0 g of 1-(4-methylbenzyl)-4-(3-chloropropyl)piperazine dihydrochloride, 6.5 g of triethylamine and 250 ml of reagent ethanol. The hydrolysis was effected with 6.0 g of sodium hydroxide in 40 ml of water. Work-up, as described above, gave 16.4 g (72% of theory) of 3-[4-(4-methylbenzyl)piperazin-1-yl] propanethiol dihydrochloride as a white crystalline solid, M.p. 273°-277° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04618677
출처 데이터셋uspto-grants-1986_10
ORD IDord-a09eccbe7ed047dd8ec4889ccede0e3a
출처 메모uspto-grants-1986_10