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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930827Generated: November 1, 2026

Diisopropylamine → 3-Fluoro-N,N-diisopropyl-5-trifluoromethyl-benzamide

https://huagongshe.com/reaction/1930827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Fluoro-5-(trifluoromethyl)benzoic acidHCID 519222—
CatalystTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product3-Fluoro-N,N-diisopropyl-5-trifluoromethyl-benzamideHCID 4420314385%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 15.9 mmol 3-Fluoro-5-(Trifluoromethyl)benzoic acid in 20 ml toluene containing 2 drops of DMF was added 79.7 mmol thionylchloride at 0° C. The mixture was heated at 85° C. for 5 hours. The solvent was carefully removed in vacuo. The colorless liquid was dissolved in 25 ml dichloromethane and cooled to 0° C. 63.8 mmol diisopropylamine was added dropwise. The mixture was allowed to warm to RT. After 1 hour the solvent was removed in vacuo. The residue was taken in ethyl acetate and washed twice with water. The washings were extracted once with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography (SiO2, heptane/ethyl acetate) to yield the title compound as a light yellow solid (85% yield). MS (m/e): 291.9 (M+, 100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188139B2
Source datasetuspto-grants-2012_05
ORD IDord-dbbaccd497274d47b7e03cb0e803411c
Source noteuspto-grants-2012_05