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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35722생성일: 2026년 10월 23일

Tetrahydrofuran → 5-(S)-methyl-7-(t-butyldimethylsilyloxy)-2-heptene

https://huagongshe.com/ko/reaction/35722

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물3-(R)-methyl-5-(t-butyldimethylsilyloxy)-1-pentanalHCID 10443866—
반응물ButyllithiumHCID 178418339—
촉매Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
용매WaterHCID 962—
생성물5-(S)-methyl-7-(t-butyldimethylsilyloxy)-2-hepteneHCID 53780377—

반응 단계

To a slurry of 80 g. (0.2155 m) of triphenyl-ethyl phosphonium bromide in 800 ml. of dry tetrahydrofuran cooled to 0° C. was added 165.7 ml. of 1.3M solution of n-butyl lithium (0.2155 m) in the same solvent. After 2 hours, 45 g. (0.196 m) 3-(R)-methyl-5-(t-butyldimethylsilyloxy)-1-pentanal in 200 ml. of dry tetrahydrofuran was added dropwise to the reaction mixture. The reaction was allowed to stir 2 hours at room temperature and was then poured into water and extracted with ether. The combined extracts were washed with water and a brine solution and dried over magnesium sulfate. Removal of the solvent in vacuo gave a yellow oil which, on distillation gave 37.4 g. of product, b.p. 74°-79° C./0.2-0.1 torr.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04767743
출처 데이터셋uspto-grants-1988_08
ORD IDord-4c5114fdff2d45a59c871c8312f0440a
출처 메모uspto-grants-1988_08