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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768878Generated: November 1, 2026

Hydrochloric Acid → 1-(4-n-Propylphenyl)-1,2,2-trifluoroethylene

https://huagongshe.com/reaction/1768878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrafluoroethyleneHCID 8301—
Reactant1-Iodo-4-propylbenzeneHCID 612541—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product1-(4-n-Propylphenyl)-1,2,2-trifluoroethyleneHCID 2009799860%

Reaction Conditions

Temperature-80 °C

Reaction Steps

In 1 l four-necked flask having a gas supplying tube, 200 ml of n-hexane, 75 ml of dry diethyl ether and 24.6 g (0.1 mol) of 4-(n-propyl)iodobenzene were introduced under a nitrogen atmosphere, and then 86.2 ml of a hexane solution of n-butyl lithium (1.16 mol) was dropwise added thereto under stirring at -80° C. Then, while the reaction system was maintained at -80° C., 10 g (0.1 mol) of tetrafluoroethylene was introduced under vigorously stirring in 30 minutes. The reaction solution was stirred further for one hour and poured into ice water and neutralized with dilute hydrochloric acid, and then the organic layer was separated. The aqueous layer was extracted with methylene chloride, and the extract was combined to the organic layer, followed by drying. The solvent was distilled off to obtain 12 g (yield: 60%) of 1-(4-n-propylphenyl)-1,2,2-trifluoroethylene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380461
Source datasetuspto-grants-1995_01
ORD IDord-8099d52e04994bb5b94ec3dd97063c50
Source noteuspto-grants-1995_01