HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 6-(Methoxymethyl)pyridin-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 10639974 | HCID 10639974 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(Methoxymethyl)pyridin-3-ol | HCID 23145775 | 59% |
Reaction Steps
Sodium methoxide (393 mg) was added to a methanol (20 ml) solution containing 5-(benzenesulfonyloxy)-2-(bromomethyl)pyridine (Beilstein Registry No. 7430370, 800 mg), followed by stirring at room temperature for 4 hours. Water was added to the reaction solution, followed by extraction with EtOAc. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: EtOAc) to obtain 6-(methoxymethyl)pyridin-3-ol (200 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919494B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-6074e52adb22490c877e928fb7edcc22 |
| Source note | uspto-grants-2011_04 |