HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Methoxy-1-benzofuran-2-carbaldehyde → (7-Methoxy-1-benzofuran-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Methoxy-1-benzofuran-2-carbaldehyde | HCID 3457310 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (7-Methoxy-1-benzofuran-2-yl)methanol | HCID 11788606 | 96.6% |
Reaction Steps
Sodium borohydride (0.462 g) was added in one portion to a stirred solution of 7-methoxybenzofuran-2-carbaldehyde (2.15 g) in methanol (50 ml) at room temperature and the reaction was stirred for 3 hours. The reaction mixture was then diluted with water (100 ml) and extracted with dichloromethane (3×30 ml). The organic extracts were combined, washed with water (30 ml), dried over magnesium sulphate, filtered and the solvent removed in vacuo to afford the title compound (2.10 g) as a pale orange liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06331556B2 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-814f83b8f41149b781400841380452c9 |
| Source note | uspto-grants-2001_12 |