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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70257생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/70257

반응식

참여 물질

역할이름HCID투입량
반응물Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate)HCID 6639—
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물TrimethylaluminumHCID 16682925—
반응물Ethyl 5-(4-hydroxyphenyl)-2-thiophene carboxylateHCID 58276533—
용매TolueneHCID 1140—
용매AcetonitrileHCID 6342—
생성물5-{4-[(2-Chloroethyl)oxy]phenyl}-2-thiophenecarboxamideHCID 58276468—

반응 조건

온도57.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822518B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3e2683c486124a4c96c2957d818c48fc
출처 메모uspto-grants-2014_09