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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2187967생성일: 2026년 10월 26일

Ammonium Chloride → (3-{(1R,2S,3R)-3-(tert-Butyldimethylsilanyloxy)-2-[(S)-(E)-3-(tert-butyldimethylsilanoxy)oct-1-enyl]-5-oxocyclopentylsulfanyl} propylsulfanyl)acetic acid methyl ester

https://huagongshe.com/reaction/2187967

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물(3S)-1-Iodo-3-(tert-butyldimethylsilyloxy)-1-octeneHCID 11111369—
반응물[3-[(R)-3-(tert-Butyldimethylsilanyloxy)-5-oxocyclopent-1-enylsulfanyl]propylsulfanyl}acetic acid methyl esterHCID 15406175—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물(3-{(1R,2S,3R)-3-(tert-Butyldimethylsilanyloxy)-2-[(S)-(E)-3-(tert-butyldimethylsilanoxy)oct-1-enyl]-5-oxocyclopentylsulfanyl} propylsulfanyl)acetic acid methyl esterHCID 1299073939%

반응 조건

온도-78 °C

반응 단계

tert-Butyllithium (1.47 mL of a 1.7M solution in pentane, 2.5 mmol) was added dropwise to a solution of tert-butyl[(S)-1-((E)-2-iodovinyl) hexyloxy]dimethylsilane 6 (462.5 mg, 1.25 mmol) in Et2O (6.0 mL) at −78° C. After stirring for 30 min lithium 2-thienylcyanocuprate (6.0 mL of a 0.25M solution in THF, 1.5 mmol) was added and the reaction was stirred an additional 30 min at −78° C. A solution of enone 5 (430 mg, 1.1 mmol) in Et2O (1 mL) was added and stirring was continued for an additional 1 h. The reaction mixture was then quickly poured into saturated aqueous NH4Cl cooled to 0° C. The mixture was extracted with EtOAc and the organic portion was washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue was quickly purified by flash column chromatography (silica gel, 100% hexane followed by 8:1 hex/EtOAc) to afford 270 mg (39%) of the above titled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06410591B1
출처 데이터셋uspto-grants-2002_06
ORD IDord-483f5741daac46f5b3a4e88673aaa685
출처 메모uspto-grants-2002_06