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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271084Generated: November 1, 2026

Butyl iodide → 7-Chloro-9-methyl-2,3,4,5-tetrahydro-1-benzoxepine

https://huagongshe.com/reaction/2271084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantSodium hydrideHCID 24758—
Reactant7-chloro-9-methyl-5-(N-ethylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepineHCID 22391793—
SolventDimethylformamideHCID 6228—
Product7-Chloro-9-methyl-2,3,4,5-tetrahydro-1-benzoxepineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333349B1
Source datasetuspto-grants-2001_12
ORD IDord-9eb08fdf4bc146858a7e141c29720522
Source noteuspto-grants-2001_12