HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710017Generated: November 1, 2026
4-Bromo-1,1,2-trifluorobut-1-ene → HCID 23035376, compound
https://huagongshe.com/reaction/1710017
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromo-1,1,2-trifluorobut-1-ene | HCID 66333 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178526642 | HCID 178526642 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23035376 | HCID 23035376 | 62.8% |
Reaction Steps
A solution of 0.25 gram (0.011 mole) of sodium in 35 ml of ethanol was stirred and 2.7 grams (0.0095 mole) of 3-(4-nitrophenylmethylthio)-5-mercapto-1,2,4-thiadiazole was added. Upon completion of addition the reaction mixture was stirred at ambient temperature for one hour. The ethanol solvent was removed under reduced pressure. The residue was dissolved in 35 ml of methyl ethyl ketone and 1.6 grams (0.0085 mole) of 4-bromo-1,1,2-trifluoro-1-butene was added. Upon completion of addition the reaction mixture was stirred for 16 hours, then was concentrated under reduced pressure to a residue. The residue was dissolved in 50 ml of toluene and washed with 25 ml of water, two 25 ml portions of aqueous 5% sodium hydroxide solution, and 25 ml of water. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to yield a residual oil. The oil was dissolved in methylene chloride and passed through a column of silica gel. The eluate was concentrated under reduced pressure to yield 2.1 grams of 3-(4-nitrophenylmethylthio)-5-(3,4,4-trifluoro-3-butenylthio)-1,2,4-thiadiazole. The nmr spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04952580 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-cb7a7e4fbd6548ba8a58fae3184962b9 |
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| Source note | uspto-grants-1990_08 |
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