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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651531Generated: October 31, 2026

Triphenylphosphine → 2-Chlorobenzenesulfonic acid 3-[(4-cyanophenyl)methoxy]-5-methylphenyl ester

https://huagongshe.com/reaction/651531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantp-Cyanobenzyl alcoholHCID 160549—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant3-(2-Chlorophenylsulfonyloxy)-5-methylphenolHCID 11277947—
SolventTetrahydrofuranHCID 8028—
Product2-Chlorobenzenesulfonic acid 3-[(4-cyanophenyl)methoxy]-5-methylphenyl esterHCID 5438880676.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diethyl azodicarboxylate (524 mg, 3.0 mmol) was added to a solution of 2-chlorobenzenesulfonic acid 3-hydroxy-5-methylphenyl ester (900 mg, 3.0 mmol), as prepared in step (c) of the Example 1, 4-cyanobenzyl alcohol (400 mg, 3.0 mmol; Yoon et al., J. Org. Chem. 38:2786-2792 (1973)), and triphenylphosphine (790 mg, 3.0 mmol) in tetrahydrofuran (20 mL) at 0° C. The mixture was stirred at 0° C. for 2 h and at room temperature for 3 h. The reaction mixture was quenched with water (50 mL) and extracted with ethyl acetate (3×50 mL). The organic phase was 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 (2:1 ethyl acetate:hexane) to give the title compound as a white solid (0.95 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281206B1
Source datasetuspto-grants-2001_08
ORD IDord-02f21d9bd9924b6eada49feacf9cccf9
Source noteuspto-grants-2001_08