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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

반응식

참여 물질

역할이름HCID투입량
반응물o-Toluenesulfonyl chlorideHCID 8623—
반응물DabcoHCID 9237—
반응물Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
용매Diethyl EtherHCID 3283—
용매tert-Butyl methyl etherHCID 15413—
생성물1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidineHCID 1064285162,906.5%

반응 조건

온도5 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642608B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-ca9cbe1d6d034a839a21db8ac3b4945c
출처 메모uspto-grants-2014_02