HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2,3,4,5-Tetrahydro-1H-3-benzazepine-7-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 7-cyano-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylate | HCID 18173275 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3,4,5-Tetrahydro-1H-3-benzazepine-7-carbonitrile | HCID 18173279 | 44% |
Reaction Steps
A mixture of 3-(tert-butyloxycarbonyl)-7-cyano-2,3,4,5-tetrahydro-1H-3-benzazepine (765 mg, 2.81 mmol) and trifluoroacetic acid (2 ml), in dichloromethane (20 ml) was stirred at 40° C. for 1 h. The reaction mixture was evaporated to dryness in vacuo and partitioned between ethyl acetate (50 ml) and water (50 ml). The aqueous layer was basified using potassium carbonate and re-extracted with ethyl acetate (2×30 ml). The combined basic organic extracts were dried over sodium sulfate and evaporated in vacuo to give the title compound as a colourless oil (212 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429579B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-3680548be0b54ada8f1c647f6c494cc6 |
| Source note | uspto-grants-2008_09 |