HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 1-(6-Bromopyridin-2-yl)-2-morpholin-4-ylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(6-Bromopyridin-2-yl)-2-morpholin-4-ylethanone | HCID 59526320 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 1-(6-Bromopyridin-2-yl)-2-morpholin-4-ylethanol | HCID 59526060 | — |
Reaction Steps
To a solution of 1-(6-bromopyridin-2-yl)-2-morpholin-4-ylethanone (234 mg, 0.82 mmol) in methanol at 0° C. was added sodium borohydride (31.0 mg, 0.82 mmol). After 30 minutes, formic acid (0.1 mL) was added and then the reaction mixture was diluted with ethyl acetate (40 mL), saturated aqueous sodium bicarbonate (10 mL), and water (10 mL). The layers were separated and the organic layer was washed with brine (10 mL), dried over sodium sulfate, filtered, and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367706B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-c55cd15ae1fc47f487154705eca98c17 |
| Source note | uspto-grants-2013_02 |