참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Trimethylsulfonium iodide | HCID 75127 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | Dtxcid5024346 | HCID 5311498 | — |
| 촉매 | Ferrous sulfate heptahydrate | HCID 62662 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Methyl Ethyl Ketone | HCID 6569 | — |
| 생성물 | CID 10898559 | HCID 10898559 | 171.4% |
반응 단계
To 260 ml of ion-exchanged water were added 20 g of cyanocobalamin, 6.02 g of trimethylsulfonium iodide and 800 mg of iron(II) sulfate heptahydrate. The mixture was heated in a water bath and, after replacing the atmosphere of the system by nitrogen, a solution of sodium borohydride (8 g)/2N sodium hydroxide (0.2 ml)/water (40 ml) and 15 ml of 2-butanone were added dropwise thereto under stirring at an inner temperature of 40° C. over 20 minutes, respectively. After stirring for 15 minutes as it was, the mixture was cooled to 15° C. Further, 15 ml of 2-butanone was added thereto, followed by stirring overnight. The precipitates were collected by filtration and dried, to give 21.4 g of a crude product of the title compound. Thereto was added 200 ml of a 50% acetone aqueous solution, and the mixture was heated, adjusted to pH 6.5 with concentrated hydrochloric acid and then filtered. After washing with 40 ml of a 50% acetone aqueous solution, 630 ml of acetone was added dropwise to the filtrate, followed by stirring at 15° C. overnight. Precipitated crystals were collected by filtration and dried, to give 17 g of the title compound (yield 86%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06657057B2 |
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| 출처 데이터셋 | uspto-grants-2003_12 |
|---|
| ORD ID | ord-1e0e0f24d4c341f8b3f1b67aac209003 |
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| 출처 메모 | uspto-grants-2003_12 |
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