HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 22767863, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22767910 | HCID 22767910 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22767863 | HCID 22767863 | — |
Reaction Steps
8.9 G. of 10,11-dihydro-2-methyl-8-methylthio-dibenz[b,f]oxepin-10-one are suspended in 65 ml. of ethanol and treated with a solution of 1.25 g. of sodium borohydride in 4.3 ml. of water. The mixture is stirred for 2 hours at room temperature. Then, 20 ml. of methanol are added thereto and the resulting mixture is heated at reflux for 15 minutes. Thereafter, the methanol and ethanol are removed by evaporation in vacuo. The residue is extracted with chloroform, the chloroform extracts are washed with water, dried and evaporated in vacuo. The residue is crystallized from diisopropyl ether, and there is obtained 10,11-dihydro- 3-methyl-8-methylthio-dibenz[b,f]oxepin- 10-ol having a melting point of 67°-69° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04032525 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-48dc95edeb00415cb1b2b4ccebdd4159 |
| Source note | uspto-grants-1977_06 |