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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2292274생성일: 2026년 10월 26일

Tetrafluoroborate → Diphenyl isopropylidene sulfurane

https://huagongshe.com/reaction/2292274

반응식

참여 물질

역할이름HCID투입량
반응물TetrafluoroborateHCID 26255—
반응물IsopropyldiphenylsulfoniumHCID 10980002—
반응물HCID 178418306HCID 178418306—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물Diphenyl isopropylidene sulfuraneHCID 11138905—

반응 조건

온도-70 °C

반응 단계

2 ml of a solution of 1.6M of tert.-butyllithium in pentane was added dropwise at -70° C. under an inert atmosphere to a stirred mixture of 950 mg of the tetrafluoroborate of isopropyldiphenylsulfonium in 15 ml of tetrahydrofuran and the mixture was stirred at -70° C. for 30 minutes to obtain a solution of diphenylisopropylidene sulfurane. The said solution at -70° C. was added slowly with stirring under an inert atmosphere to a mixture of 350 mg of 5(RS) methoxy-2,5-dihydrofuran-2-one [prepared by method of Schroeter et al, Liebigs Ann. Chem., Vol. 697 (1966), p. 42] and 15 ml of tetrahydrofuran cooled to -90° C. and the mixture was allowed to stand at -78° C. for one hour and then at -50° C. for another hour. The mixture was poured into an aqueous monosodium phosphate solution and the mixture was extracted with methylene chloride. The organic phase was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with a 1-1 ether-petrolum ether mixture yielded 480 mg of diphenyl sulfide, 260 mg of (1RS, 5SR) 6,6-dimethyl-4(RS)-methoxy-3-oxabicyclo [3,1,0]-hexan-2-one and 100 mg of unreacted lactone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04801723
출처 데이터셋uspto-grants-1989_01
ORD IDord-e2c2153fb24f4e1397c5354808fd68af
출처 메모uspto-grants-1989_01