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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976105Generated: November 1, 2026

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

https://huagongshe.com/reaction/1976105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl esterHCID 54263647—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product2-Chlorobenzenesulfonic acid 3-hydroxyphenyl esterHCID 5401528196.6%

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225302B1
Source datasetuspto-grants-2001_05
ORD IDord-11058eecc161474eb9c2ff2e7f15bb79
Source noteuspto-grants-2001_05