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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453553Generated: October 26, 2026

Dichloromethane → Tert-butyl 2-(4-(4-((2,4-dichlorophenethyl)carbamoyl)phenoxy)-3-cyanophenyl)propanoate

https://huagongshe.com/reaction/453553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(4-chlorophenethyl)-4-hydroxybenzamideHCID 60628097—
ReactantTert-butyl 2-(3-cyano-4-fluorophenyl)propanoateHCID 68467119—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 2-(4-(4-((2,4-dichlorophenethyl)carbamoyl)phenoxy)-3-cyanophenyl)propanoateHCID 68466062—

Reaction Conditions

Temperature95 °C

Reaction Steps

A flask was charged with tert-butyl 2-(3-cyano-4-fluorophenyl)propanoate (0.07 g), N-(4-chlorophenethyl)-4-hydroxybenzamide (0.105 g), and potassium carbonate (0.047 g) in 1 ml of DMSO and stirred at 95° C. for one day. The reaction was taken up in dichloromethane and washed with water. The organic layer was collected, dried over MgSO4, filtered, and concentrated. The crude material was purified by silica gel chromatography, eluting with a solvent system of 5%-80% ethyl acetate/hexanes gave tert-butyl 2-(4-(4-((2,4-dichlorophenethyl)carbamoyl)phenoxy)-3-cyanophenyl)propanoate (0.102 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492437B2
Source datasetuspto-grants-2013_07
ORD IDord-5b81197b8d634a7cbf4712bfae5cada5
Source noteuspto-grants-2013_07