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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531068Generated: October 30, 2026

Hydrogen Bromide → 2,2',4'-Trifluoro-3-hydroxybiphenyl-4-carbaldehyde

https://huagongshe.com/reaction/531068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant2,2',4'-Trifluoro-3-methoxybiphenyl-4-carbaldehydeHCID 117992089—
SolventAcetic AcidHCID 176—
Product2,2',4'-Trifluoro-3-hydroxybiphenyl-4-carbaldehydeHCID 11799215694.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

48% hydrobromic acid (22.0 mL) was added at room temperature to an acetic acid (120 mL) solution of 2,2′,4′-trifluoro-3-methoxybiphenyl-4-carbaldehyde (5.14 g), and the mixture was stirred at 120° C. for 16 hours in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and then, the solvent was distilled off under reduced pressure. The obtained residue was neutralized with a 1 M aqueous sodium hydroxide solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with water and saturated saline in this order and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was passed through a short silica gel column (hexane/ethyl acetate) to obtain the title compound (4.60 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353108B2
Source datasetuspto-grants-2016_05
ORD IDord-bda3e6209bb24521a5f819dd115cb76f
Source noteuspto-grants-2016_05