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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant4,4,4-TrifluorobutanalHCID 2777083—
Solvent1,4-DioxaneHCID 31275—
Product2-Bromo-4,4,4-trifluorobutyraldehydeHCID 5808114076.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785486B2
Source datasetuspto-grants-2014_07
ORD IDord-ed28eb7d81014ee1a439bdc3c9c4dc4d
Source noteuspto-grants-2014_07