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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221589생성일: 2026년 10월 23일

Potassium Carbonate → (R)-1-(Tetrahydro-2H-pyran-4-yl)ethane-1,2-diol

https://huagongshe.com/ko/reaction/221589

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-EthenyloxaneHCID 12411805—
반응물2-Methylpropan-2-ol--water (1/1)HCID 71401949—
촉매TolueneHCID 1140—
촉매HCID 178511488HCID 178511488—
용매DichloromethaneHCID 6344—
생성물(R)-1-(Tetrahydro-2H-pyran-4-yl)ethane-1,2-diolHCID 67156576—

반응 조건

온도0 °C

반응 단계

A 500-mL, round-bottomed flask was charged with potassium ferricyanide (III) (15.0 g, 45.6 mmol), 2,5-diphenyl-4,6-bis(9-O-dihydroquinidyl)pyrimidine ((DHQD)2-PYR) (132 mg, 0.15 mmol) and K2CO3 (6.29 g, 45.6 mmol). A 1:1 mixture of tert-butyl alcohol/H2O (150 mL) was added and the suspension was stirred under N2. A 0.25 M solution of OSO4 in toluene (0.60 mL, 0.15 mmol) was then added the mixture was cooled to 0° C. After stirring for 60 minutes, 4-vinyltetrahydro-2H-pyran (1.70 g, 15.2 mmol) was added and the mixture was stirred overnight. Solid Na2S2O5 (22.5 g) was then added and the reaction mixture was allowed to warm to ambient temperature. CH2Cl2 (150 mL) was then added and the layers were separated. The aqueous layer was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave 2.11 g of (1R)-1-tetrahydro-2H-pyran-4-ylethane-1,2-diol as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207162B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-01b62622e18d4355b62ba8d1da07e78b
출처 메모uspto-grants-2012_06