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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514898Generated: November 3, 2026

3-Chlorobenzotrifluoride → 2-Chloro-6-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/1514898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorobenzotrifluorideHCID 7374—
ReactantMethyl formateHCID 7865—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-Chloro-6-(trifluoromethyl)benzaldehydeHCID 17750679—

Reaction Steps

To a solution of 1-chloro-3-trifluoromethylbenzene (1.0 g, 5.54 mmol) in THF (15 mL) cooled to −78° C., under N2 protection was added dropwise n-BuLi (3.81 mL of a 1.6 M solution in hexane, 6.1 mmol). After an hour, formic acid methyl ester (664.8 mg, 11.08 mmol) was added slowly to the solution. After the addition, the solution was warmed to ambient temperature slowly and stirred for 30 min. The reaction mixture was quenched with water and the aqueous layer was extracted with EtOAc. The organic layer was washed with water, brine, dried with MgSO4 and filtered. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using heptane/EtOAc (15:1) as eluent to give 2-chloro-6-trifluoromethylbenzaldehyde as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222248B2
Source datasetuspto-grants-2012_07
ORD IDord-ecdac2f096c449f8933712c7b067454a
Source noteuspto-grants-2012_07