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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1590945생성일: 2026년 10월 25일

Tributylstannane → 4-Benzoyloxy-1-t-butoxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/1590945

반응식

참여 물질

역할이름HCID투입량
반응물TributylstannaneHCID 5948—
반응물2-Iodo-2-methylpropaneHCID 11206—
반응물1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 688178—
용매ChlorobenzeneHCID 7964—
생성물4-Benzoyloxy-1-t-butoxy-2,2,6,6-tetramethylpiperidineHCID 1299690744.5%

반응 단계

A solution of 56.0 g (203 mmol) of 4-benzoyloxy-1-oxyl-2,2,6,6-tetramethylpiperidine, 125 ml of chlorobenzene, and 58.9 g of t-butyl iodide is cooled to 5° C. Tri-n-butyltin hydride (29 g, 100 mmol) is added dropwise over 110 minutes while the temperature is maintained below 20° C. The reaction mixture is concentrated at reduced pressure and then purified by silica gel chromatography (200:1, then 100:3 heptane:ethyl acetate) to afford 30.1 g of a white solid, m.p. 80°-82.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05204473
출처 데이터셋uspto-grants-1993_04
ORD IDord-03b8a0f652b34942ad38273eb81f18a7
출처 메모uspto-grants-1993_04