HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841834Generated: November 3, 2026
Water → 1-[(E)-1,2-difluoro-2-(4-propylcyclohexyl)vinyl]-4-ethoxy-2,3-difluorobenzene
https://huagongshe.com/reaction/1841834
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | B-(4-Ethoxy-2,3-difluorophenyl)boronic acid | HCID 15135235 | — |
| Reactant | 1-((Z)-1,2-difluoro-2-iodovinyl)-4-propylcyclohexane | HCID 86674303 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | 1-[(E)-1,2-difluoro-2-(4-propylcyclohexyl)vinyl]-4-ethoxy-2,3-difluorobenzene | HCID 67327725 | — |
Reaction Steps
6.30 g (20.1 mmol) of 1-((Z)-1,2-difluoro-2-iodovinyl)-4-propylcyclohexane and 4.86 g (24.1 mmol) of 2,3-difluoro-4-ethoxybenzeneboronic acid are refluxed for 19 h together with 1.16 g (1.0 mmol) of tetrakistriphenylpalladium(0) and 20 ml (20 mmol) of sodium carbonate solution (2 M) in 90 ml of ethanol/toluene (2:1). Water is added, and the batch is extracted with MTBE. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with water. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:1-chlorobutane=4:1). The further purification is carried out by recrystallisation from n-heptane, giving 1-[(E)-1,2-difluoro-2-(4-propylcyclohexyl)vinyl]-4-ethoxy-2,3-difluorobenzene as a colourless solid (m.p. 60° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08945420B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-e459ec64e4d5444990b74c50d79fdd09 |
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| Source note | uspto-grants-2015_02 |
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