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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271082Generated: October 31, 2026

Triethylamine → 7-chloro-9-methyl-5-(N-ethylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepine

https://huagongshe.com/reaction/2271082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant5-Amino-7-chloro-9-methyl-2,3,4,5-tetrahydro-1-benzoxepineHCID 22391789—
SolventTetrahydrofuranHCID 8028—
Product7-chloro-9-methyl-5-(N-ethylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepineHCID 2239179385.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333349B1
Source datasetuspto-grants-2001_12
ORD IDord-2395683f46e5417698c5c6252117a9e5
Source noteuspto-grants-2001_12