HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352413Generated: October 30, 2026
Hydrochloric Acid → 3-Bromo-4-n-butoxy-1,1,1-trifluorobut-3-en-2-one
https://huagongshe.com/reaction/2352413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Butoxyvinyl trifluoromethyl ketone | HCID 2782641 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 3-Bromo-4-n-butoxy-1,1,1-trifluorobut-3-en-2-one | HCID 54022425 | — |
Reaction Steps
8.0 g (0.05 mole) of bromine, dissolved in 100 ml pentane, are added dropwise to a solution of 9.75 g (0.05 mol) of 4-n-butoxy-1,1,1-trifluorobut-3-en-2-one in 50 ml of pentane cooled to -20° C. After stirring for 1 hour at -20° C., a solution of 6.0 g (0.06 mole) of triethylamine in 100 ml pentane is added dropwise at the same temperature. After being allowed to stand overnight at 25° C., the mixture is poured into ice water and acidified by means of 1N hydrochloric acid and the phases are separated. Conventional work-up gives 12.1 g of almost homogeneous crude 3-bromo-4-n-butoxy-1,1,1-trifluorobut-3-en-2-one, which is freed from the small amount of impurities by distillation under reduced pressure. Boiling point 113°-115° C./16 mbar, nD20 =1.4640.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04876393 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-c4781c4695bd4daa887c88383a984d49 |
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| Source note | uspto-grants-1989_10 |
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