Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651535Generated: October 30, 2026

2-Chlorobenzenesulfonyl chloride → 2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl ester

https://huagongshe.com/reaction/651535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl 3-hydroxyphenyl etherHCID 138048—
SolventDichloromethaneHCID 6344—
Product2-Chlorobenzenesulfonic acid 3-benzyloxyphenyl esterHCID 5426364795.2%

Reaction Steps

3-Benzyloxyphenol (2.97 g, 15 mmol), as prepared in the preceding step, in methylene chloride (50 mL) was treated with diisopropylethylamine (2 mL) and 2-chlorobenzenesulfonyl chloride (3.27 g, 15.5 mmol) at 0° C. for 2 h and at room temperature for 2 h. The reaction mixture was diluted with 200 mL of methylene chloride, washed sequentially with saturated NaHCO3 (2×50 mL) and brine (2×50 mL), and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by flash column chromatography (1:1 hexane:methylene chloride) to give the title compound as a colorless liquid (5.35 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281206B1
Source datasetuspto-grants-2001_08
ORD IDord-fd747ac063474b179c5db12e6841cbc6
Source noteuspto-grants-2001_08