HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600467Generated: October 29, 2026
Triphenylphosphine → HCID 178455762, compound
https://huagongshe.com/reaction/1600467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Tribromofluoromethane | HCID 67707 | — |
| Reactant | HCID 178455770 | HCID 178455770 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 178455762 | HCID 178455762 | — |
Reaction Steps
A solution of tribromofluoromethane and triphenyl phosphine in ethylene glycol dimethyl ether was stirred at 70° C. for 1 hour. The reaction solution was cooled with ice, and a solution of trans-4-(trans-4-ethylcyclohexyl)cyclohexane carboaldehyde in tetrahydrofuran was added thereto. After the reaction solution was further stirred for 1 hour, the temperature of the solution was gradually raised up to room temperature, and insoluble substances were removed by filtration. Dilute hydrochloric acid was added to the filtrate, and it was extracted with toluene. After the organic layer was washed with water, it was dried by using anhydrous magnesium sulfate, and concentrated under a reduced pressure to obtain a brown oily product. After this product was purified by using a silica gel column chromatography, it was recrystallized from heptane to obtain trans-4-(trans-4-ethylcyclohexyl)cyclohexyl-2-fluoro-2-bromoethene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05976408 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-0ef7506cc8324ddcb4daf9be46433a35 |
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| Source note | uspto-grants-1999_11 |
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