HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → 7-Chloro-2,3,4,5-tetrahydro-1-benzoxepin-9-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 2,3,4,5-Tetrahydro-1-benzoxepin-9-carboxylic acid | HCID 12701150 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Chloro-2,3,4,5-tetrahydro-1-benzoxepin-9-carboxylic acid | HCID 14502097 | — |
Reaction Steps
To a solution of 1.7 g (8.9 mmol) of 2,3,4,5-tetrahydro-1-benzoxepin-9-carboxylic acid in 5 ml of DMF is added 1.41 g(10.6 mmol) of N-chlorosuccinimide (NCS) in one portion at room temperature. The solution is stirred overnight and then diluted with ethyl acetate and washed with water. The organic layer is then dried (MgSO4), filtered and concentrated to obtain 7-chloro-2,3,4,5-tetrahydro-1-benzoxepin-9-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04924010 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-bf635fa7ecbc469db7d164f8e9c7fec1 |
| Source note | uspto-grants-1990_05 |