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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271079Generated: October 26, 2026

Methyl iodide → 5-(N-methyl-N-methylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepine

https://huagongshe.com/reaction/2271079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-Methylsulfonylamino-2,3,4,5-tetrahydro-1-benzoxepineHCID 22391790—
SolventTetrahydrofuranHCID 8028—
Product5-(N-methyl-N-methylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepineHCID 2239178031.6%

Reaction Steps

A solution of 1.1 g (6.2 mmol) of 5-methylsulfonylamino-2,3,4,5-tetrahydro-1-benzoxepine in 15 ml of THF was added dropwise to a suspension of 0.23 g (6.2 mmol) of 80 percent sodium hydride in 10 ml of THF. After 2 h at RT, 0.94 g (6.7 mmol) of iodomethane were added and the mixture was stirred overnight at RT. After distilling off the solvent in vacuo, the residue was taken up in EA, and the solution was washed with dilute hydrochloric acid and water, dried over magnesium sulfate and concentrated. Subsequent recrystallization of the product from isopropanol yielded 0.5 g of 5-(N-methyl-N-methylsulfonylamino)-2,3,4,5-tetrahydro-1-benzoxepine, m.p. 143-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333349B1
Source datasetuspto-grants-2001_12
ORD IDord-709884320e994b2db490e34751abb95b
Source noteuspto-grants-2001_12