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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880260Generated: October 31, 2026

Water → HCID 86631570, compound

https://huagongshe.com/reaction/1880260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
Reactant5-Bromo-1,3-dichloro-2-(difluoromethoxy)benzeneHCID 66865742—
ReactantHCID 178477747HCID 178477747—
SolventDimethylformamideHCID 6228—
ProductHCID 86631570HCID 86631570—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 21 mL of a 1M tetrahydrofuran solution of 1-trifluoromethylethenyl zinc bromide prepared according to a method described in the literatures, a solution of 2.4 g of 4-bromo-2,6-dichloro(difluoromethoxy)benzene in 12 mL of N,N-dimethylformamide was added, and tetrahydrofuran was distilled off under reduced pressure. To the remaining N,N-dimethylformamide solution, 0.23 g of dichlorobis(triphenylphosphine) palladium (II) was added and the resultant mixture was stirred at 100° C. for 3 hours. After the completion of the reaction, the reaction mixture was left to be cooled down to room temperature and charged into 100 mL of water and the resultant mixture was extracted with diethyl ether (100 mL×1). The organic phase was washed with water and then dehydrated and dried over saturated saline and anhydrous sodium sulfate in this order and the solvent was distilled off under reduced pressure. The resultant residue was purified by silica gel column chromatography eluting with hexane to obtain 1.8 g of the objective substance as a brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318757B2
Source datasetuspto-grants-2012_11
ORD IDord-2aa98a461fd64f7a8dbbb2af06e61cd7
Source noteuspto-grants-2012_11