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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880257Generated: November 2, 2026

Tetrahydrofuran → HCID 66865196, compound

https://huagongshe.com/reaction/1880257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant5-Bromo-2,3-dichlorotolueneHCID 641158—
ReactantTetrahydrofuran hexaneHCID 21883165—
ReactantHCID 178477747HCID 178477747—
SolventDimethylformamideHCID 6228—
ProductHCID 66865196HCID 66865196—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a nitrogen atmosphere, to 19 mL of a 1M tetrahydrofuran solution of 1-trifluoromethylethenyl zinc bromide prepared according to a method described in the literatures, a solution of 2.2 g of 5-bromo-2,3-dichlorotoluene in 10 mL of N,N-dimethylformamide was added and tetrahydrofuran was distilled off under reduced pressure. To the remaining N,N-dimethylformamide solution, 0.26 g of dichlorobis(triphenylphosphine) palladium (II) was added and the resultant mixture was stirred at 100° C. for 3.5 hours. After the completion of the reaction, the reaction mixture was left to be cooled down to room temperature and 200 mL of a tetrahydrofuran-hexane (2:5) mixture was added to the reaction mixture, followed by filtering off the deposited insoluble substance. The resultant filtrate was washed with water (100 mL×1) 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 2.3 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-8338cd4a7523407aa0f379938d050ca7
Source noteuspto-grants-2012_11