HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767140Generated: October 31, 2026
Thionyl Chloride → (E)-2-(3-Chloroprop-1-en-1-yl)-1,4-difluorobenzene
https://huagongshe.com/reaction/1767140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,5-Difluorocinnamyl alcohol | HCID 53401580 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-2-(3-Chloroprop-1-en-1-yl)-1,4-difluorobenzene | HCID 11608064 | 100% |
Reaction Steps
A solution of 0.34 cm3 (4.66 mmol) of thionyl chloride and 0.555 g (4.66 mmol) of benzotriazole in 40 cm3 of dichloromethane is added at a temperature in the region of 20° C. under an argon atmosphere to 0.646 g (3.8 mmol) of 2,5-difluorocinnamyl alcohol in solution in 40 cm3 of dichloromethane. After stirring for 10 minutes, the reaction mixture is filtered on No. 3 sintered glass and the solid residue rinsed with twice 10 cm3 of dichloromethane. The filtrate is washed 3 times with 30 cm3 of water. The organic phase is dried over magnesium sulfate and filtered to give a solution of 2-[(1E)-3-chloro-1-propenyl]-1,4-difluorobenzene (3.8 mmol) which is then concentrated to dryness under reduced pressure (2.7 kPa) at a temperature in the region of 20° C., before dissolution in acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07232833B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-1c690237919a464298268cc1a552fd28 |
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| Source note | uspto-grants-2007_06 |
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