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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 470164생성일: 2026년 10월 24일

Water → (3aS,4S,6aR)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-ol

https://huagongshe.com/ko/reaction/470164

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium borohydrideHCID 4311764—
반응물(3aR,6aR)-2,2-dimethyl-hexahydrocyclopenta(d)(1,3)dioxol-4-oneHCID 11171111—
용매MethanolHCID 887—
생성물(3aS,4S,6aR)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-olHCID 58329311—

반응 단계

(3 aR,6aR)-2,2-dimethyldihydro-3 aH-cyclopenta[d][1,3]dioxol-4(5H)-one (1-2) (2.75 g, 17.6 mmol, 1 equiv) was dissolved in methanol (166 mL) and sodium borohydride (1.0 g, 26.4 mmol, 1.5 equiv) was added portion wise at 0° C. Upon disappearance of the starting material as monitored by LC-MS analysis, water was added and the mixture was concentrated. The aqueous phase was extracted with DCM (3×100 mL), the combined organics were dried (Na2SO4), and the solvent was removed to afford (3AS,4S,6aR)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-ol (1-3) as a colorless oil that did not require further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629275B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-da1b85dbb0ba4c429867c590c47a462a
출처 메모uspto-grants-2014_01