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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1636504생성일: 2026년 10월 26일

2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl ester → 2-Chlorobenzenesulfonic acid 3-hydroxyphenyl ester

https://huagongshe.com/reaction/1636504

반응식

참여 물질

역할이름HCID투입량
반응물2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl esterHCID 54263647—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물2-Chlorobenzenesulfonic acid 3-hydroxyphenyl esterHCID 5401528196.6%

반응 단계

2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl ester (3.75 g, 10 mmol), as prepared in the preceding step, Pd/C (10%) (350 mg) in tetrahydrofuran (80 mL) was hydrogenated balloon) for 3 h. The catalyst was filtered through Celite and washed with tetrahydrofuran. The combined tetrahydrofuran solution was evaporated in vacuo and the residue was then purified by flash column chromatography (methylene chloride) to give the title compound as a colorless oil (2.75 g, 95%). 1H-NMR (300 MHz, CDCl3) δ 6.68 (m, 3H), 7.12 (t, 1H, J=6.5 Hz), 7.37 (t, 1H, J=7.1 Hz), 7.60 (m, 2H), 7.94 (dd, 1H, J=0.6, 4.0 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06034127
출처 데이터셋uspto-grants-2000_03
ORD IDord-419e35e221ba4e549739011ad3e56805
출처 메모uspto-grants-2000_03