돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520392생성일: 2026년 10월 24일

Trimethylsilyl triflate → HCID 86690105, 화합물

https://huagongshe.com/ko/reaction/520392

반응식

참여 물질

역할이름HCID투입량
반응물Trimethylsilyl triflateHCID 65367—
반응물2,2,7,7-Tetramethyl-3,6-dioxa-2,7-disilaoctaneHCID 81858—
반응물Ethyl 5-oxooctahydropentalene-2-carboxylateHCID 73030532—
용매DichloromethaneHCID 6344—
생성물HCID 86690105HCID 86690105—

반응 조건

온도-78 °C

반응 단계

To a solution of ethyl 5-oxooctahydropentalene-2-carboxylate (210 mg) in DCM (5 mL) cooled to −78° C. were added slowly trimethylsilyl trifluoromethanesulfonate (11.89 mg, 0.054 mmol) and 2,2,7,7-tetramethyl-3,6-dioxa-2,7-disilaoctane (287 mg, 1.391 mmol) under nitrogen. After stirring at −78° C. for 30 min, the reaction mixture was warmed to rt and stirred at rt for 16 h. The reaction was quenched with anhydrous pyridine at −78° C. followed by sat. NaHCO3, and then extracted with EtOAc. The combined organic layers were dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography to afford ethyl hexahydro-1′H-spiro[[1,3]dioxolane-2,2′-pentalene]-5′-carboxylate (a mixture of endo/exo isomers) as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09326973B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-e79d6d27da3542bbb9b8e6cfad961f63
출처 메모uspto-grants-2016_05