HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (6-(Benzyloxy)pyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-(Benzyloxy)nicotinaldehyde | HCID 21102205 | — |
| Solvent | Water | HCID 962 | — |
| Product | (6-(Benzyloxy)pyridin-3-yl)methanol | HCID 59255139 | 91.1% |
Reaction Steps
To a methanol (20.0 mL) solution of 6-benzyloxy-pyridine-3-carbaldehyde (2.00 g, 9.38 mmol) described in Manufacturing Example 12-1-2 was added sodium borohydride (426 mg, 11.3 mmol) on an ice bath (0° C.) under nitrogen atmosphere, which was stirred for 10 minutes at room temperature. Water was added to the reaction mixture at room temperature, which was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure to obtain the title compound (1.84 g, 91.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691882B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-04fef0959752458fb46f7ad90ebca9fa |
| Source note | uspto-grants-2010_04 |