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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361740Generated: October 31, 2026

Bromine → 2-Bromo-4,4,4-trifluorobutyraldehyde

https://huagongshe.com/reaction/2361740

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., bromine (2.24 ml, 43.65 mmol) was added 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 D4 (6.2 g, 76%) that was used in the next reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691813B2
Source datasetuspto-grants-2014_04
ORD IDord-b900e6d946eb4e79b7397e274629fbd3
Source noteuspto-grants-2014_04