Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238087생성일: 2026년 10월 25일
o-Toluenesulfonyl chloride → 1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidine
https://huagongshe.com/reaction/238087
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | o-Toluenesulfonyl chloride | HCID 8623 | — |
| 반응물 | Dabco | HCID 9237 | — |
| 반응물 | Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 2764081 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | 1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidine | HCID 10642851 | 62,906.5% |
반응 단계
1,4-Diazabicyclo[2.2.2]octane (42.4 g, 0.378 mol) was added to a solution of 1-(tert-butoxycarbonyl)-4-hydroxymethylpiperidine (52.5 g, 0.244 mol) in tert-butyl methyl ether (525 ml). After stiffing for 15 minutes at ambient temperature, the mixture was cooled to 5° C. and a solution of toluene sulphonyl chloride (62.8 g, 0.33 mmol) in tert-butyl methyl ether (525 ml) was added in portions over 2 hours while maintaining the temperature at 0° C. After stirring for 1 hour at ambient temperature, petroleum ether (1 l) was added. The precipitate was removed by filtration. The filtrate was evaporated to give a solid. The solid was dissolved in ether and washed successively with 0.5N aqueous hydrochloric acid (2×500 ml), water, saturated sodium hydrogen carbonate and brine, dried (MgSO4) and evaporated to give 1-(tert-butoxycarbonyl)-4-(4-methylphenylsulphonyloxymethyl)piperidine (76.7 g, 85%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642608B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-ca9cbe1d6d034a839a21db8ac3b4945c |
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| 출처 메모 | uspto-grants-2014_02 |
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