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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244298생성일: 2026년 10월 25일

4-Methylmorpholine → 4,5-Dibromo-1,2-cyclohexanediol

https://huagongshe.com/reaction/244298

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물MAGNESIUM SILICATE (synthetic)HCID 61680—
반응물4,5-Dibromocyclohex-1-eneHCID 112470—
반응물Sodium BisulfiteHCID 23665763—
촉매Osmium TetroxideHCID 30318—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물4,5-Dibromo-1,2-cyclohexanediolHCID 12885764—

반응 단계

The compound obtained in Step (9) (80.5 g, 338 mmol), water (500 ml), acetone (250 ml), and N-methylmorpholine (45.5 g, 389 mmol) were placed in a reaction vessel, and was stirred. OsO4 (1 g) was added to the mixture, and was vigorously stirred for 24 hours. After the completion of the reaction, a suspension of NaHSO3 (50 g) and Florisil (250 g) in water (100 ml) was added to the reaction solution, and was stirred for 10 minutes. After that, insoluble matter was removed by celite filtration, and 5% HCl was added to the filtrate until the pH of the filtrate became 3. Upon confirming that the pH had reached 3, and acetone was removed under reduced pressure. Organic matter was extracted from the remainder with ethyl acetate, dried over sodium sulfate, and concentrated under reduced pressure. The precipitated crystals were filtrated, and was then recrystallized with methylene chloride, whereby 4,5-dibromo-1,2-cyclohexanediol was obtained (64.6 g, 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658459B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-0e346a26936e43e8b847368d383dbaef
출처 메모uspto-grants-2014_02