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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927741Generated: October 31, 2026

Potassium Carbonate → Methyl 2-(4-(4-((4-chlorophenethyl)carbamoyl)-2-nitrophenoxy)-3-fluorophenyl)acetate

https://huagongshe.com/reaction/1927741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-(4-chlorophenethyl)-4-chloro-3-nitrobenzamideHCID 4810824—
ReactantMethyl 2-(3-fluoro-4-hydroxyphenyl)acetateHCID 10797559—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-(4-((4-chlorophenethyl)carbamoyl)-2-nitrophenoxy)-3-fluorophenyl)acetateHCID 6846704446.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 2-(3-fluoro-4-hydroxyphenyl)acetate (prepared in Step A; 163 mg, 0.885 mmol) was diluted with DMSO (3 mL) followed by the addition of K2CO3 (122 mg, 0.885 mmol) and N-(4-chlorophenethyl)-4-chloro-3-nitrobenzamide (prepared in Step B; 300 mg, 0.885 mmol). The reaction was stirred at 80° C. for 12 hours. The reaction was cooled, diluted with DCM and washed with 10% aq. sodium carbonate, water and brine. The layers were separated and the organic layer was dried over MgSO4, filtered and concentrated. The material was purified by silica gel chromatography, eluting with hexane:acetone (2:1) to yield methyl 2-(4-(4-((4-chlorophenethyl)carbamoyl)-2-nitrophenoxy)-3-fluorophenyl)acetate (200 mg, 46.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183289B2
Source datasetuspto-grants-2012_05
ORD IDord-635cbc9f17d1403f84dc11e57811b2d3
Source noteuspto-grants-2012_05