HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → 1-(6-Bromopyridin-3-yl)-2-methoxyethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(6-Bromopyridin-3-yl)-2-methoxyethan-1-one | HCID 59331558 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(6-Bromopyridin-3-yl)-2-methoxyethanol | HCID 59331580 | 96% |
Reaction Steps
To a mixture of 1-(6-bromopyridin-3-yl)-2-methoxyethanone (15.85 g), tetrahydrofuran (15 mL) and ethanol (15 mL) was slowly added sodium borohydride (0.97 g) at room temperature, and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added 10% aqueous citric acid solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography, and the title compound (15.26 g, yield 96%) was obtained as a yellow oil from a fraction eluted with ethyl acetate. MS: 234 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318746B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-a5de980d5da344ef97f42271328f69f8 |
| Source note | uspto-grants-2012_11 |