돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356445생성일: 2026년 10월 24일

Thionyl Chloride → 5-Chloro-N-hydroxy-N-(1-methylethyl)-3-(trimethylsilyl)-2-thiophenecarboxamide

https://huagongshe.com/ko/reaction/356445

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물N-Isopropylhydroxylamine HydrochlorideHCID 170873—
반응물Sodium BicarbonateHCID 516892—
반응물5-Chloro-3-(trimethylsilyl)-2-thiophenecarboxylic acidHCID 18630239—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물5-Chloro-N-hydroxy-N-(1-methylethyl)-3-(trimethylsilyl)-2-thiophenecarboxamideHCID 12039976—
생성물5-Chloro-3-(trimethylsilyl)-2-thiophenecarboxylic acid chlorideHCID 54024836—

반응 단계

5-Chloro-3-(trimethylsilyl)-2-thiophenecarboxylic acid chloride was prepared by the reaction of 1 g 5-chloro-3-(trimethylsilyl)-2-thiophenecarboxylic acid (prepared as in Example 263) and 6 mL thionyl chloride, using the procedure of step a in Example 248. This product was dissolved in CH2Cl2 at 0° C. and added to a mixture of N-isopropylhydroxylamine hydrochloride (0.55 g, 5 mmol) and 4 g NaHCO3 in 20 mL CH2Cl2 and 20 mL water. The resulting reaction mixture was stirred at RT for additional 3 h. The organic layer was separated, washed with brine, dried and concentrated. The residue was purified by flash chromatography with 8% ethyl acetate/hexane to give 80 mg of the title compound. m.p. 146°-150° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834447
출처 데이터셋uspto-grants-1998_11
ORD IDord-8896cf152ec648a5b5ab47a50bf1258a
출처 메모uspto-grants-1998_11