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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1,1,2-trifluorobut-1-eneHCID 66333—
ReactantSodiumHCID 5360545—
ReactantHCID 178526642HCID 178526642—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 23035376HCID 2303537662.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952580
Source datasetuspto-grants-1990_08
ORD IDord-cb7a7e4fbd6548ba8a58fae3184962b9
Source noteuspto-grants-1990_08