HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl iodide → 7-Chloro-9-methyl-2,3,4,5-tetrahydro-1-benzoxepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-chloro-9-methyl-5-(N-ethylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepine | HCID 22391793 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Chloro-9-methyl-2,3,4,5-tetrahydro-1-benzoxepine | HCID 131723051 | — |
Reaction Steps
A solution of 0.8 g (2.6 mmol) of 7-chloro-9-methyl-5-(N-ethylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepine (Example 10c) in 10 ml of DMF was added dropwise under nitrogen to a suspension of 0.1 g (2.7 mmol) of 80 percent sodium hydride in 8 ml of DMF. After stirring at RT for 30 min, 0.68 g (3.7 mmol) of butyl iodide was added dropwise and the mixture was additionally stirred overnight at RT. After distilling off the solvent, the residue was treated with water and extracted with EA. After washing the organic phase with dil. hydrochloric acid in water, and drying over magnesium sulfate, it was concentrated in vacuo. 0.9 g of 5-N-butyl-N-ethylsulfonylamino)-7-chloro-9-methyl-2,3,4,5-tetrahydro-1-benzoxepine was obtained, m.p. 83-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06333349B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-9eb08fdf4bc146858a7e141c29720522 |
| Source note | uspto-grants-2001_12 |