돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2222183생성일: 2026년 10월 26일

Benzoyl chloride → 1-Benzoyl-3-[2-methoxy-5-(tetrahydropyran-4-yl)-phenyl]-thiourea

https://huagongshe.com/reaction/2222183

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물AmthioHCID 13417437—
반응물2-Methoxy-5-(tetrahydropyran-4-yl)-phenylamineHCID 21919262—
용매AcetoneHCID 180—
생성물1-Benzoyl-3-[2-methoxy-5-(tetrahydropyran-4-yl)-phenyl]-thioureaHCID 2271957166%

반응 단계

To a stirred solution of 1.11 g (14.6 mmol) ammonium rhodanide in 60 ml acetone was added dropwise 1.54 ml (13.3 mmol) benzoyl chloride and the mixture heated at reflux for 10 minutes. A solution of 2.75 g (13.3 mmol) 2-methoxy-5-(tetrahydro-pyran-4-yl)-phenylamine in 30 ml acetone was then added dropwise and the reaction mixture heated at reflux for a further 10 minutes. The mixture was then cooled to room temperature, poured onto sodium bicarbonate solution, and extracted three times with dichloromethane. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. Flash chromatography (1/1 ethyl acetate/hexane) followed by trituration in ether afforded 3.25 g (66%) 1-benzoyl-3-[2-methoxy-5-(tetrahydro-pyran-4-yl)-phenyl]-thiourea as a white solid. ES-MS m/e (%): 371 (M+H+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07371748B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-b2c28496b1374d5ba70bbf58c28fede4
출처 메모uspto-grants-2008_05