HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-hydroxymethylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Formylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one | HCID 18422140 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-hydroxymethylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one | HCID 18422152 | 62% |
Reaction Steps
2-Formylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one (1.6 g) was suspended in methanol (30 ml) and sodium borohydride (480 mg) was added. The mixture was stirred at room temperature for 1.5 hours. The reaction mixture was diluted with water and extracted 3 times with chloroform. The organic layer was dried over sodium sulfate and the solvent was evaporated under reduced pressure. To the residue were added chloroform and diisopropyl ether and the precipitated crystals were collected by filtration to give 2-hydroxymethylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one (1.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455521B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-bbae3245b4314f84ae17d176b46eac19 |
| Source note | uspto-grants-2002_09 |