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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28099Generated: October 28, 2026

Potassium Carbonate → 2-Fluoro-5-phenoxybenzyl 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylate

https://huagongshe.com/reaction/28099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHexamethylphosphoramideHCID 12679—
Reactant2-Fluoro-5-phenoxybenzyl bromideHCID 14579132—
Reactant3-(4-Chlorophenoxy)-2,2-dimethylcyclopropanecarboxylic acidHCID 20304961—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-5-phenoxybenzyl 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylateHCID 54440629—

Reaction Steps

To a mixture of 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylic acid (2.77 mmol), potassium carbonate (3.25 mmol) and hexamethylphosphoric triamide (HMPT) (3 ml), with stirring and under nitrogen, at RT, is added 2-fluoro-5-phenoxybenzyl bromide (2.77 mmol) in THF. The reaction is stirred at RT for about 48 hours and then worked up by partition between water/ether. The organic phase is washed with water and brine, dried over potassium carbonate, filtered and the solvent is removed from the filtrate. The residue is plated on prep. TLC plates developing with 10% ether/hexane to yield 2-fluoro-5-phenoxybenzyl 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225533
Source datasetuspto-grants-1980_09
ORD IDord-bd1c0c1c5b2d448aa9897a4eb2fd9cf3
Source noteuspto-grants-1980_09