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HRID 2271077作成日:2026年10月27日

Methyl iodide → 5-(N-ethylsulfonyl-N-methylamino)-2,3,4,5-tetrahydro-1-benzoxepine

https://huagongshe.com/reaction/2271077

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物5-Ethylsulfonylamino-2,3,4,5-tetrahydro-1-benzoxepineHCID 22391808—
溶媒TetrahydrofuranHCID 8028—
生成物5-(N-ethylsulfonyl-N-methylamino)-2,3,4,5-tetrahydro-1-benzoxepineHCID 1543453395.2%

反応手順

A solution of 1.0 g (3.9 mmol) of 5-ethylsulfonylamino-2,3,4,5-tetrahydro-1-benzoxepine in 15 ml of THF were added dropwise under nitrogen to a suspension of 0.16 g (5.4 mmol) of 80 percent sodium hydride in 10 ml of THF. After stirring at RT for 3 h, 1.6 g (11 mmol) of methyl iodide were 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. The organic phase was concentrated in vacuo after drying over sodium sulfate. 1.0 g of 5-(N-ethylsulfonyl-N-methylamino)-2,3,4,5-tetrahydro-1-benzoxepine was obtained, m.p. 122-124° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06333349B1
出典データセットuspto-grants-2001_12
ORD IDord-a6dc94c4fe4b4a9fbe05f414a473c68f
出典メモuspto-grants-2001_12