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HRID 70257作成日:2026年10月26日

Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → 5-{4-[(2-Chloroethyl)oxy]phenyl}-2-thiophenecarboxamide

https://huagongshe.com/reaction/70257

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate)HCID 6639—
反応物Potassium CarbonateHCID 11430—
反応物Ammonium ChlorideHCID 25517—
反応物TrimethylaluminumHCID 16682925—
反応物Ethyl 5-(4-hydroxyphenyl)-2-thiophene carboxylateHCID 58276533—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
生成物5-{4-[(2-Chloroethyl)oxy]phenyl}-2-thiophenecarboxamideHCID 58276468—

反応条件

温度57.5 °C

反応手順

To a suspension of ammonium chloride (2.12 g, 39.6 mmol) in 10 ml of toluene at 5° C. was added dropwise 19.8 ml of 2M trimethylaluminum in toluene solution. The mixture was stirred for 2 h at the room temperature and ethyl 5-(4-hydroxyphenyl)-2-thiophene carboxylate (Intermediate KK-1-1) (1.98 g, 7.03 mmol) was added. The resulting mixture was heated at 55-60° C. for 15 h, cooled to 5° C. and quenched with ethanol (10 ml). All solvents were removed in vacuo and the residue was treated with 80 ml of 0.5M HCl solution. A yellow solid was collected by filtration, washed with water and air-dried (1.64 g). The product was added to a mixture of 2-chloroethyl p-toluenesulfonate (4.07 ml, 22.5 mmol) and potassium carbonate (3.11 g, 22.5 mmol) in 100 ml of acetonitrile. After heating at reflux for 40 h, the reaction mixture was filtered to remove the solids, concentrated to dryness in vacuo and purified by silica gel column chromatography using Hexanes and EtOAc to give the title compound as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822518B2
出典データセットuspto-grants-2014_09
ORD IDord-3e2683c486124a4c96c2957d818c48fc
出典メモuspto-grants-2014_09