HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050529Generated: November 2, 2026
4-Bromo-1,1,2-trifluorobut-1-ene → HCID 20058441, compound
https://huagongshe.com/reaction/2050529
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-1,1,2-trifluorobut-1-ene | HCID 66333 | — |
| Reactant | HCID 178527953 | HCID 178527953 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20058441 | HCID 20058441 | 1,594.3% |
Reaction Steps
2.1 g (0.019 mol) of potassium t-butylate are introduced into a solution of 3.2 g (0.018 mol) of 2-mercapto-5-(tetrahydrofuran-2-yl)-1,3,4-oxadiazole in a mixture of 80 ml of 1,4-dioxane and 10 ml of dimethylformamide. 4.9 g (0.026 mol) of 1-bromo-3,4,4-trifluoro-3-butene are then added dropwise at 25° C. and the reaction mixture is stirred at room temperature for 16 hours. The solvent mixture is distilled off under reduced pressure and the residue is dissolved in ethyl acetate. This solution is extracted with water, ice-cold 1 N sodium hydroxide solution and water in succession, dried with sodium sulfate and filtered and the solvent is distilled off under reduced pressure. 80.43 g of the desired product are obtained as a yellow oil (nD27 =1.4904).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05013745 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-9ff02882986d4ee9a174a9261d262df3 |
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| Source note | uspto-grants-1991_05 |
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