돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 482087생성일: 2026년 10월 25일

2-Chlorobenzenesulfonic acid 3-benzyloxy-5-methylphenyl ester → 3-(2-Chlorophenylsulfonyloxy)-5-methylphenol

https://huagongshe.com/reaction/482087

반응식

참여 물질

역할이름HCID투입량
반응물2-Chlorobenzenesulfonic acid 3-benzyloxy-5-methylphenyl esterHCID 19064976—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물3-(2-Chlorophenylsulfonyloxy)-5-methylphenolHCID 11277947—

반응 단계

A mixture of 2-chlorobenzenesulfonic acid 3-benzyloxy-5-methylphenyl ester (4.66 g, 12 mmol), as prepared in the preceding step, and 10% palladium on carbon (500 mg) in tetrahydrofuran (80 mL) was hydrogenated (balloon) for 3 h. The catalyst was removed by filtration through diatomaceous earth (tetrahydrofuran washes) and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography (methylene chloride) to give the title compound as a pale-yellow solid (3.20 g, 89%, 1 H-NMR (300 MHz, CDCl3) δ 2.22 (s, 3H), 5.24 (s, 1H), 6.44 (t, 1H), 6.53 (d, 2H), 7.38 (dt, 1H), 7.60 (m, 2H), 7.96 (dd, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05792769
출처 데이터셋uspto-grants-1998_08
ORD IDord-c8cec32e717c49cda57606d7deda4967
출처 메모uspto-grants-1998_08