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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395414Generated: October 30, 2026

Potassium Carbonate → HCID 53800296, compound

https://huagongshe.com/reaction/395414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromineHCID 24408—
ReactantHCID 22668796HCID 22668796—
ReactantHCID 69880965HCID 69880965—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 53800296HCID 5380029680%

Reaction Steps

To a solution of 18.0 g(49.3 mmol) of methyl 4-(cyclopropylmethyl)-2-(difluoromethyl)-5-(2-methoxyethenyl)-6-(trifluoromethyl)-3-pyridinecarboxylate (example 127 of U.S. Pat. No. 6,169,432) in 250 ml of ether was added 7.9 g (49.4 mmol) of bromine. The reaction mixture was stirred at room temperature for 2 h and to the mixture was added 6.8 g of freshly ground potassium carbonate and 100 ml of methanol. The reaction mixture was stirred for another 45 min and was washed with water and brine. The organic layer was dried (MgSO4), filtered through celite, and concentrated in vacuo. The residue was kugelrohr distilled and the distillate was purified by chromatography (7% EtOAc in hexane) to give 18.7 g (80% yield) of 1:1 mixture of methyl 5-(1-bromo-2,2-dimethoxyethyl)-4-(cyclopropylmethyl)-2-(difluoromethyl)-6-(trifluoromethyl)-3-pyridinecarboxylate and product. HPLC purification (10% EtOAc in hexane) gave 4.1 g of the desired product as a colorless oil which crystallized and was recrystallized from hexane to give crystals, mp 79-79.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605624B1
Source datasetuspto-grants-2003_08
ORD IDord-b25e177f67c34280b7338afb46f1dc0c
Source noteuspto-grants-2003_08