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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | 1-Iodo-4-propylbenzene | HCID 612541 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-(4-n-Propylphenyl)-1,2,2-trifluoroethylene | HCID 20097998 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380461 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-8099d52e04994bb5b94ec3dd97063c50 |
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| Source note | uspto-grants-1995_01 |
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