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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 368544생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/368544

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, 3 H), 7.12 (t, 1H, J=6.5 Hz), 7.37 (t, 1H, J=7.1 Hz), 7.60 (m, 2 H), 7.94 (dd, 1H, J=0.6, 4.0 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06133315
출처 데이터셋uspto-grants-2000_10
ORD IDord-fdea59b8637546e0b6774de4ed7839b7
출처 메모uspto-grants-2000_10