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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46101생성일: 2026년 10월 23일

Tetrahydrofuran → (1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diol

https://huagongshe.com/ko/reaction/46101

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Carbamide PeroxideHCID 31294—
반응물(1R,2S,4R,5S)-2,5-bis(trimethoxysilyl)bicyclo[2.2.1]heptaneHCID 11439107—
반응물Potassium fluoride, 99%, spray-driedHCID 53443437—
촉매Manganese dioxideHCID 14801—
용매MethanolHCID 887—
생성물(1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diolHCID 9989289—

반응 조건

온도60 °C

반응 단계

To (1R,2S,4R,5S)-2,5-bis(trimethoxysilyl)bicyclo[2.2.1]heptane (76.9 mmol) was added potassium hydrogen fluoride (33.0 g, 423 mmol), tetrahydrofuran (80.0 mL), methanol (80.0 mL), and urea hydrogen peroxide addition compound (65.0 g, 691 mmol, Aldrich). The resulting white slurry was stirred overnight at 60° C. After cooling to ambient temperature, MnO2 (0.56 g, 6.4 mmol) was added, and the mixture was stirred at this temperature for 4 h. The solids were removed by filtration, and the filter cake was washed with methanol. The combined filtrates were concentrated in vacuo. The residue was dissolved in water (100 mL) and extracted with a CHCl3/i-PrOH mixture (3/1, v/v, 5×100 mL). The combined organic portions were dried over MgSO4 and conc. in vacuo. After triturating the residue with CH2Cl2 and EtOAc, the white solid was collected by filtration. This material was the title compound. A second crop of desired product was obtained by flash column chromatography (0-5% MeOH in EtOAc) from the concentrated filtrate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541592B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-db2dfc9685ae4cd1916f84e301b6a968
출처 메모uspto-grants-2013_09