HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-chloro-9-methyl-5-(N-ethylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | 5-Amino-7-chloro-9-methyl-2,3,4,5-tetrahydro-1-benzoxepine | HCID 22391789 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-chloro-9-methyl-5-(N-ethylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepine | HCID 22391793 | 85.8% |
Reaction Steps
0.86 g of ethanesulfonyl chloride was added dropwise with ice-cooling to a solution of 1.3 g of 5-amino-7-chloro-9-methyl-2,3,4,5-tetrahydro-1-benzoxepine and 2.4 g of triethylamine in 30 ml of THF. The mixture was allowed to come to room temperature and was stirred overnight, and the solvent was distilled off in vacuo. After stirring the residue with water, the deposited product was filtered off with suction and dried in vacuo. 1.6 g of 7-chloro-9-methyl-5-(N-ethylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepine were obtained, m.p. 144-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06333349B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-2395683f46e5417698c5c6252117a9e5 |
| Source note | uspto-grants-2001_12 |