HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-(6-Chloropyrimidin-4-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(6-Chloropyrimidin-4-yl)ethan-1-one | HCID 72214247 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(6-Chloropyrimidin-4-yl)ethanol | HCID 83854101 | 79.7% |
Reaction Steps
1-(6-Chloro-4-pyrimidinyl)ethanone (Intermediate 18A, 1.0 g, 6.39 mmol) was dissolved in ethanol (21 mL), treated with sodium borohydride (0.242 g, 6.39 mmol) and the resulting mixture was stirred at room temperature under argon for 2 hours. The solvent was removed under reduced pressure and the residue was diluted with water and extracted with ethyl acetate (×3). The ethyl acetate layers were combined, dried under magnesium sulfate and evaporated under reduced pressure to give the title compound as a yellow oil (808 mg);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796283B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-e2acdec75d9640a7ac4fac48b35ea0e7 |
| Source note | uspto-grants-2014_08 |