HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 7-Bromo-2,3,4,5-tetrahydro-1H-1-benzazepine-9-carboxylic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-bromo-2,3,4,5-tetrahydro-1H-1-benzazepine-9-carboxylic acid | HCID 10199296 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Bromo-2,3,4,5-tetrahydro-1H-1-benzazepine-9-carboxylic acid benzyl ester | HCID 53645003 | 99.7% |
Reaction Steps
To 7-bromo-2,3,4,5-tetrahydro-1H-1-benzazepine-9-carboxylic acid (8.53 g) dissolved in DMF (80 ml), were added potassium carbonate (13.8 g) and benzyl bromide (4.5 ml) and the mixture was stirred for 2 hours at room temperature. After the insoluble matter was filtered off and the filtrate was concentrated, a mixed liquid of ethyl acetate-benzene (1:1, 400 ml) was added to the residue, and the mixture was washed with water, dried over anhydrous sodium sulfate and then subjected to distilling off the solvent to give the intended compound 11.35 g (99.7%) as brown oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05242912 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-53267f682d9a4174af11e039aaa24acc |
| Source note | uspto-grants-1993_09 |