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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 855986생성일: 2026년 10월 24일

Pyridine → 5-[4-(4-tert-Butyl-phenoxy)-phenylsulfamoyl]-2-methyl-benzoic acid

https://huagongshe.com/ko/reaction/855986

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-(4-Tert-butylphenoxy)anilineHCID 82498—
반응물5-(Chlorosulfonyl)-2-methylbenzoic acidHCID 308449—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물5-[4-(4-tert-Butyl-phenoxy)-phenylsulfamoyl]-2-methyl-benzoic acidHCID 5893704082%

반응 단계

A solution of 4-(4-tert-butyl-phenoxy)-phenylamine (0.1 g, 0.41 mmol). 5-chlorosulfonyl-2-methylbenzoic acid (0.097 g, 0.41 mmol) and pyridine (0.1 ml, 1.24 mmol) in 2 ml anhydrous tetrahydrofuran was heated at 60° C. for 2 hr. The reaction mixture was cooled to room temperature and diluted with 30 ml ethyl acetate. The ethyl acetate solution was washed sequentially with 25 ml 1N aqueous hydrochloric acid solution and 25 ml brine, dried (anhydrous sodium sulfate) and concentrated to dryness under reduced pressure. The crude product was purified by preparative thick layer chromatography (silica gel), eluting with 9:1 chloroform/methanol to yield the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07262318B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-d16715c87bba49a5856bec6decc7aad8
출처 메모uspto-grants-2007_08