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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52387생성일: 2026년 10월 24일

Toluene → 1,2,2,6,6-Pentamethyl-4-(oxiran-2-ylmethoxy)piperidine

https://huagongshe.com/ko/reaction/52387

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물EpichlorohydrinHCID 7835—
반응물Sodium HydroxideHCID 14798—
반응물4-Piperidinol, 1,2,2,6,6-pentamethyl-HCID 75472—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
생성물1,2,2,6,6-Pentamethyl-4-(oxiran-2-ylmethoxy)piperidineHCID 14274505—

반응 단계

300 g (7.5 mol) of sodium hydroxide are dissolved in 300 g of water under an argon atmosphere in a 2.5 l sulfonation flask fitted with mechanical stirrer, condenser and 500 l dropping funnel. 750 ml of toluene, 48.4 g (0.15 mol) of tetrabutylammonium bromide and 257 g (1.5 mol) of 4-hydroxy-1,2,2,6,6-pentamethylpiperidine are added. 347 g of epichlorohydrin (3.75 mol) are added dropwise at 60° C. over the course of 1.5 hours, and the mixture is subsequently stirred at the same temperature for a further 4 hours. The reaction solution is poured in 3 l of ice water, and the organic phase is separated off, dried using sodium sulfate and evaporated. The residue is distilled at 0.05 mmHg over a Vigreux column, and the fraction of boiling point 71°-72° C. is collected. Yield: 205 g (60%). GC: >99%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616637
출처 데이터셋uspto-grants-1997_04
ORD IDord-313ddd5281a040698a4b9baad84c5756
출처 메모uspto-grants-1997_04