Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trimethyloxosulphonium chloride | HCID 197819 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Dtxcid5024346 | HCID 5311498 | — |
| Catalyst | Ferrous sulfate heptahydrate | HCID 62662 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | CID 10898559 | HCID 10898559 | 179.9% |
Reaction Steps
To 130 ml of ion-exchanged water were added 10 g of cyanocobalamin, 2.85 g of trimethylsulfoxonium chloride, 700 mg of iron (II) sulfate heptahydrate and 7.5 ml of 2-butanone. After replacing the atmosphere of the system by nitrogen, the mixture was heated in a water bath. A solution of sodium borohydride (4 g)/2N sodium hydroxide (0.5 ml)/water (20 ml) was added dropwise thereto under stirring at an inner temperature of 35° C. After stirring for 3 hours as it was, the mixture was cooled to 15° C. and then stirred overnight. Thereto was added 7.5 ml of butanone, followed by stirring for 2 hours. Then, the precipitates were collected by filtration and dried, to give 35 g of a crude product of the title compound. Thereto was added 140 ml of a 50% acetone aqueous solution. The mixture was heated at 45° C., filtered and washed with 60 ml of a 50% acetone aqueous solution. After the mixture was adjusted to pH 6.5 with concentrated hydrochloric acid, 475 ml of acetone was added dropwise thereto and the mixture was stirred at 20° C. overnight. Precipitated crystals were collected by filtration and dried, to give 8.92 g of the title compound (yield 89.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06657057B2 |
|---|
| Source dataset | uspto-grants-2003_12 |
|---|
| ORD ID | ord-13d54ad2ba3d42278ad544b30b5bf738 |
|---|
| Source note | uspto-grants-2003_12 |
|---|