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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1921961생성일: 2026년 10월 27일

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/1921961

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참여 물질

역할이름HCID투입량
반응물PentaneHCID 8003—
반응물1-(Trimethylsilyl)prop-1-yneHCID 80363—
반응물N,N,N',N'-TetramethylethanediamineHCID 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 μL) 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 번호US08173810B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-d0785bb3a6df4a7f9518a3ae0ef123f8
출처 메모uspto-grants-2012_05