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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1810857생성일: 2026년 10월 27일

Chlorosuccinimide → 2-Chloro-5-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/1810857

반응식

참여 물질

역할이름HCID투입량
반응물ChlorosuccinimideHCID 31398—
반응물m-Chlorophenethylic alcoholHCID 78856—
반응물Methyl 3-hydroxy-4-methoxybenzoateHCID 4056967—
반응물3-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl esterHCID 67076296—
촉매Zirconium chloride (ZrCl4), (T-4)-HCID 9856075—
용매DichloromethaneHCID 6344—
생성물2-Chloro-5-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl esterHCID 67076336—

반응 단계

Methyl 3-hydroxy-4-methoxybenzoate and 2-(3-chlorophenyl)-ethanol were reacted in analogy to step 1 of example 1. The obtained 3-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester (300 mg, 0.935 mmol), N-chloro-succinimide (381 mg, 2.81 mmol), and zirconium tetrachloride (129 mg, 0.57 mmol) were suspended in DCM (4 ml) and the mixture was stirred under reflux for 5 h until the starting material was used up. The mixture was partitioned between EA and a saturated aqueous sodium hydrogencarbonate solution, the aqueous phase extracted with EA, and the combined organic extracts were dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by silica chromatography (HEP/EA gradient) to give 118 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362073B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-1f56a12b3a5f4d8d9d4bc253fdcd92dd
출처 메모uspto-grants-2013_01