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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473384생성일: 2026년 10월 25일

Pentane → (S)-N-((2S,3S)-1,2-bis(tert-butyldimethylsilyloxy)-6-(trimethylsilyl)hex-5-yn-3-yl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/473384

반응식

참여 물질

역할이름HCID투입량
반응물PentaneHCID 8003—
반응물1-(Trimethylsilyl)prop-1-yneHCID 80363—
반응물N~1~,N~1~,N'~1~,N'~1~-Tetramethylethane-1,1-diamineHCID 17803068—
반응물(NE,S)-N-[(2S)-2,3-bis[[tert-butyl(dimethyl)silyl]oxy]propylidene]-2-methylpropane-2-sulfinamideHCID 44239381—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물(S)-N-((2S,3S)-1,2-bis(tert-butyldimethylsilyloxy)-6-(trimethylsilyl)hex-5-yn-3-yl)-2-methylpropane-2-sulfinamideHCID 86627014—

반응 조건

온도-78 °C

반응 단계

Trimethyl(prop-1-ynyl)silane (4 mL, 28 mmol) and N,N,N′,N′-tetramethylethanediamine (5 mL, 36 mmol) were dissolved in dry diethyl ether (50 mL) and cooled to −78° C. Tert-butyllithium, 1.7 M solution in pentane (17 mL, 28 mmol) was added dropwise and the heterogenous solution was allowed to warm to 0° C. for 15 min to give a clear yellow solution, which was recooled to −78 C. Azeotropically (S,E)-N—((S)-2,3-bis(tert-butyldimethylsilyloxy)propylidene)-2-methylpropane-2-sulfinamide (3.0 g, 7 mmol) in dry THF (20 mL) was added dropwise and the solution was stirred for 1 h until the starting material was consumed. The reaction mixture as quenched with NH4Cl and extracted with EtOAc. The combined organics were washed with water, brine, dried over Na2SO4, filtered, and concentrated to afford a yellow oil as (S)—N-((2S,3S)-1,2-bis(tert-butyldimethylsilyloxy)-6-(trimethylsilyl)hex-5-yn-3-yl)-2-methylpropane-2-sulfinamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633315B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-9362f4e4f81c41a1b262d3a38a89967f
출처 메모uspto-grants-2014_01