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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453536Generated: October 26, 2026

Potassium Carbonate → tert-Butyl 2-(4-(4-(4-chlorophenethylcarbamoyl)phenoxy)-3-cyanophenyl)acetate

https://huagongshe.com/reaction/453536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 45925946HCID 45925946—
ReactantN-(4-chlorophenethyl)-4-hydroxybenzamideHCID 60628097—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 2-(4-(4-(4-chlorophenethylcarbamoyl)phenoxy)-3-cyanophenyl)acetateHCID 6846717940%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of tert-butyl 2-(3-cyano-4-fluorophenyl)acetate (1.32 g, 5.59 mmol), N-(4-chlorophenethyl)-4-hydroxybenzamide (1.85 g, 671 mmol), and potassium carbonate (0.93 g, 6.70 mmol) in DMSO (10 ml) was stirred at 90° C. for 1 day. The reaction was cooled, diluted with ethyl acetate, and washed with 10% aqueous Na2CO3. The aqueous layer was back extracted with ethyl acetate. The organic washes were combined, washed with 10% Na2CO3 and brine, dried over sodium sulfate and concentrated. The crude material was purified by silica gel chromatography, eluting with a gradient of 5% ethyl acetate/hexanes to 60% ethyl acetate/hexanes gave tert-butyl 2-(4-(4-((4-chlorophenethyl)carbamoyl)phenoxy)-3-cyanophenyl)acetate (1.09 g, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492437B2
Source datasetuspto-grants-2013_07
ORD IDord-49a01a6ed93c4c6d8fca67880f261b1a
Source noteuspto-grants-2013_07