참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | MAGNESIUM SILICATE (synthetic) | HCID 61680 | — |
| 반응물 | 4,5-Dibromocyclohex-1-ene | HCID 112470 | — |
| 반응물 | Sodium Bisulfite | HCID 23665763 | — |
| 촉매 | Osmium Tetroxide | HCID 30318 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4,5-Dibromo-1,2-cyclohexanediol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08658459B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-0e346a26936e43e8b847368d383dbaef |
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| 출처 메모 | uspto-grants-2014_02 |
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