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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1350832생성일: 2026년 10월 25일

4-tert-Butylphenoxyacetyl chloride → 2-(4-tert-Butylphenoxy)-N-{4-[(methylsulfonyl)amino]benzyl}acetamide

https://huagongshe.com/reaction/1350832

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-Butylphenoxyacetyl chlorideHCID 611195—
반응물4-(Methylsulfonylamino)benzylamine hydrochlorideHCID 2760996—
용매PyridineHCID 1049—
생성물2-(4-tert-Butylphenoxy)-N-{4-[(methylsulfonyl)amino]benzyl}acetamideHCID 2109747362%

반응 단계

To a stirred pyridine (15 ml) suspension of N-[4-(aminomethyl)-phenyl]methane sulfonamide hydrochloride (376 mg, 1.59 mmol) was added (4-tert-butylphenoxy)acetic acid chloride (300 mg, 1.3 mmol) at 0° C. and the mixture was stirred for 1 hour at ambient temperature. The reaction was then partitioned with ethylacetate and 2M aqueous solution of hydrogen chloride and the organic layer was separated, washed with brine, dried over magnesium sulfate. Then, filtration to remove magnesium sulfate, evaporation under reduced pressure gave the residue, which was applied to a silica gel chromatography column and eluted with a volume mixture of hexane/ethylacetate (1/1 to 1/2) to furnish 240 mg (62% yield) of title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07214824B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-5fd021b3f8ac4d209bdb3045e6c68dbe
출처 메모uspto-grants-2007_05