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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170944Generated: October 30, 2026

Isopropanol → 4-Bromo-2-(trifluoromethoxy)benzaldehyde

https://huagongshe.com/reaction/2170944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantN-FormylmorpholineHCID 20417—
Reactant4-Bromo-2-(trifluoromethoxy)iodobenzeneHCID 2736422—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Bromo-2-(trifluoromethoxy)benzaldehydeHCID 18700087—

Reaction Conditions

Temperature-78 °C

Reaction Steps

20.00 g (54.51 mmol) of 4-bromo-2-(trifluoromethoxy)iodobenzene are dissolved in 200 ml of THF and cooled to −78° C. Then 26.16 ml (65.41 mmol) of a 2.5 M solution of n-butyllithium in hexane are added dropwise. The mixture is stirred for 30 min and then 14.43 g (125.37 mmol) of N-formylmorpholine are metered in. After complete conversion is detected (TLC check), solvolysis is carried out at −78° C. with isopropanol. Warming to room temperature is followed by addition of water and extraction twice with dichloromethane. The combined organic phases are washed with saturated sodium chloride solution and dried with sodium sulfate, and the solvent is distilled out under reduced pressure. The residue is purified by column chromatography (silica gel, mobile phase: cyclohexane/ethyl acetate 5:1). 11.43 g (78% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051316B2
Source datasetuspto-grants-2015_06
ORD IDord-d005ac4e7bf548bc8a15c6d08e9f513d
Source noteuspto-grants-2015_06