HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 12330038, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl (11-oxo-6,11-dihydrodibenzo[b,e]oxepin-2-yl)acetate | HCID 10333952 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12330038 | HCID 12330038 | — |
Reaction Steps
A solution of 1.4 g. of sodium borohydride, 200 ml. of methanol, and 4.0 g. of methyl 6,11-dihydro-11-oxodibenz[b,e]oxepin-2-acetate is stirred at 5°-10° for four hours and then the methanol is removed under high vacuum. Water and tetrahydrofuran are added to the residue, and the solution is adjusted to a pH of 5-6 with the addition of acetic acid and stirred for two hours at room temperature. The mixture is extracted with chloroform, and the chloroform solution is dried over sodium sulfate and concentrated. Trituration of the solid with ether provides methyl 6,11-dihydro-11-hydroxydibenz[b,e]oxepin-2-acetate as colorless crystals, m.p. 85°-87°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816591 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-1280a5f7f35b48b4a309abadb4c6d3f3 |
| Source note | uspto-grants-1989_03 |