HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 13490388, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Cyano-8-fluorodibenzo[b,f]thiepine | HCID 13490387 | — |
| Product | HCID 13490388 | HCID 13490388 | — |
Reaction Steps
Suspend 300 mg. of the cyano compound of Step 1 in 8 ml. of 20% aqueous sodium hydroxide and 8 ml. of absolute ethanol. Reflux under nitrogen for 2 hours. Evaporate the ethanol. Acidify the suspension with 20% hydrochloric acid and separate the solids by filtration. Dissolve the residue in 20 ml. of hot methanol and add a few drops of concentrated hydrochloric acid. Evaporate the methanol, dilute with ether and evaporate again. Dilute with water, stir for 30 minutes, and filter. Wash the solids with water and dry in vacuo at 100° C. to obtain the title product (m.p., 270°-272° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536507 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-68682442c730484fad02e543696ae126 |
| Source note | uspto-grants-1985_08 |