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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257270생성일: 2026년 10월 23일

Toluene → 1,2-Decanediol

https://huagongshe.com/ko/reaction/257270

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물1-DeceneHCID 13381—
반응물Sodium SulfiteHCID 24437—
촉매Osmium TetroxideHCID 30318—
촉매HCID 178511488HCID 178511488—
용매Ethyl AcetateHCID 8857—
용매2-Methylpropan-2-ol--water (1/1)HCID 71401949—
생성물1,2-DecanediolHCID 7914183.2%

반응 조건

온도0 °C

반응 단계

To a well-stirred solution of bis-1,4-(9'-O-dihydroquinidine)phthalazine (7.8 mg, 0.01 mmol), potassium ferricyanide (0.99 g, 3 mmol), potassium carbonate (0.42 g, 3 mmol), and osmium tetroxide (0.1 mL of a 0.1M toluene solution, 0.01 mmol) in 15 mL of a tert-butyl alcohol-water (1:1, v/v) at 0° C., 1-decene (0.14 g, 0.19 mL, 1 mmol) was added in one portion. The mixture was stirred for 24 h at 0° C. Solid sodium sulfite (1.5 g) was added and the mixture was stirred for an additional hour, and then warmed up to room temperature. Ethyl acetate (10 mL) was added to the reaction mixture, and aqueous layer was extracted with ethyl acetate (3×5 mL). Combined organic layer was dried over anhydrous magnesium sulfate, and concentrated in vacuo. Crude product was purified by flash chromatography (silica gel, hexanes/EtOAc) to afford decane 1,2-diol as a white solid (0.145 g, 83%). HPLC analysis of the bis-Mosher ester of this crude decane 1,2 diol gave 84% ee.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05260461
출처 데이터셋uspto-grants-1993_11
ORD IDord-5d317fd0c8aa4f019316bfb9a8cfe508
출처 메모uspto-grants-1993_11