HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627015Generated: October 31, 2026
Bromine → 2-Bromo-4,4,4-trifluorobutyraldehyde
https://huagongshe.com/reaction/1627015
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4,4,4-Trifluorobutanal | HCID 2777083 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Bromo-4,4,4-trifluorobutyraldehyde | HCID 58081140 | 76.2% |
Reaction Steps
To a mixture of 4,4,4-trifluorobutyraldehyde (5 g, 39.68 mmol) in 1,4-dioxane (5 ml) cooled to 0° C., was added bromine (2.24 ml, 43.65 mmol), dropwise. The reaction mixture was stirred at 0° C. for 2 h. The resulting reaction mixture was filtered through a pad of diatomaceous earth and the filtrate was washed with NaHCO3 (aqueous sat. solution). The organic layer was separated, dried (MgSO4) and evaporated in vacuo to yield compound D8 (6.2 g, 76%) that was used in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785486B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-ed28eb7d81014ee1a439bdc3c9c4dc4d |
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| Source note | uspto-grants-2014_07 |
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