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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 715975생성일: 2026년 10월 24일

Tributyltin Chloride → Tert-butyl 2-tributylstannanylethynylpyrrolidine-1-carboxylate

https://huagongshe.com/ko/reaction/715975

반응식

참여 물질

역할이름HCID투입량
반응물Tributyltin ChlorideHCID 15096—
반응물tert-Butyl 2-ethynylpyrrolidine-1-carboxylateHCID 14730283—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 2-tributylstannanylethynylpyrrolidine-1-carboxylateHCID 7098458461.2%

반응 조건

온도-30 °C

반응 단계

n-Butyllithium (1.6M in hexanes, 12.3 mL) was added over 2 minutes to a stirred solution of tert-butyl 2-ethynylpyrrolidine-1-carboxylate (3.65 g) in anhydrous THF (80 mL) at −78° C. under nitrogen and then the mixture was allowed to warm to −30° C. over one hour. Tributyltin chloride (6.41 g) was then added dropwise at −30° C. and the mixture was allowed to warm to −10° C. and quenched by addition of saturated sodium bicarbonate solution. The layers were separated and the organic layer was dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-5% to give tert-butyl 2-tributylstannanylethynylpyrrolidine-1-carboxylate (5.54 g) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09187494B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-776f43b0be0942e2b951c2f0e804c936
출처 메모uspto-grants-2015_11