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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105840Generated: October 30, 2026

Chlorosulfonyl isocyanate → 5-Cyano-2-ethoxy-4-methoxy-benzoic acid ethyl ester

https://huagongshe.com/reaction/2105840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant2-Ethoxy-4-methoxybenzoic acid ethyl esterHCID 67071501—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Cyano-2-ethoxy-4-methoxy-benzoic acid ethyl esterHCID 6887144954%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirring solution of 2-ethoxy-4-methoxy-benzoic acid ethyl ester (1.5 g, 6.7 mmol) in 1,2-dichloroethane (2 mL) was added chlorosulfonyl isocyanate (0.923 mL, 10.6 mmol, in 1 mL of 1,2-dichloroethane) in several portions. The reaction was stirred at 50° C. overnight. Reaction was diluted with methylene chloride (2 mL) and water (1 mL), and extracted. The organic layer was washed with brine and concentrated in vacuo. Purification of the crude residue by flash column chromatography (silica gel, eluting with a gradient of ethyl acetate in hexanes) gave 900 mg (54% yield) of 5-cyano-2-ethoxy-4-methoxy-benzoic acid ethyl ester. LC-MS: 236.2 [(M+H—CH3)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579368B2
Source datasetuspto-grants-2009_08
ORD IDord-3963d5147c654160b6625bd750ffcdcd
Source noteuspto-grants-2009_08