HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydrido[tris(methanolato)]borate(1-) → HCID 18440784, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydrido[tris(methanolato)]borate(1-) | HCID 3084262 | — |
| Reactant | HCID 18440775 | HCID 18440775 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18440784 | HCID 18440784 | 85.4% |
Reaction Steps
A solution of the product of Example 2 (20 mg, 0.05 mmol) in dichloromethane (2 mL) was treated with cyclohexaldehyde (3 mg, 0.07 mmol) and sodium trimethoxyborohydride (9 mg, 0.07 mmol). The solution was stirred at room temperature for 4 hours. The mixture was diluted with water and extracted with ethyl acetate. The aqueous layer was separated and extracted with additional ethyl acetate, the organic layers were combined, dried over anhydrous magnesium sulphate, filtered and concentrated at reduced pressure. The residue was chromatographed on a Gilson HPLC to give the title compound (10 mg, 40%) as a yellow solid; MS(ES) m/e 469 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189745B1 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-f156611ac9ad4424be1e86b01db296c5 |
| Source note | uspto-grants-2007_03 |