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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412078Generated: October 25, 2026

Chloroform → 4-(Dichloromethyl)-2-fluoro-5-nitrobenzotrifluoride

https://huagongshe.com/reaction/412078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant2-Fluoro-5-nitrobenzotrifluorideHCID 94954—
ReactantAcetic acid methanolHCID 10129899—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product4-(Dichloromethyl)-2-fluoro-5-nitrobenzotrifluorideHCID 1853674851.2%

Reaction Steps

To a solution of potassium t-butoxide (1.25 g, 11.1 mmol) in tetrahydrofuran (25 ml) was slowly added dropwise a solution of 2-fluoro-5-nitrobenzotrifluoride (1.00 g, 4.78 mmol) and chloroform (599 mg, 5.02 mmol) in tetrahydrofuran (2.5 ml) at −78° C. After stirring for 15 minutes at the same temperature, acetic acid-methanol (1:1, 5 ml) was added and the temperature was raised to room temperature. Ethyl acetate and saturated brine were added to the reaction mixture, which was extracted with ethyl acetate. After washed with brine, the organic layer was dried over anhydrous magnesium sulfate and solvent was distilled off. The residue obtained was submitted to silica gel column chromatography [hexane→hexane-ethyl acetate(300:1)] to obtain 714 mg of title compound as pale yellow liquid. Yield 51%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562839B1
Source datasetuspto-grants-2003_05
ORD IDord-709a237c3984425b80c000aa069b163e
Source noteuspto-grants-2003_05