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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411214Generated: November 1, 2026

Toluene → 3-(Trifluoromethyl)benzenepropanal

https://huagongshe.com/reaction/1411214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium SulfateHCID 24436—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantMethyl 3-[3-(trifluoromethyl)phenyl]propanoateHCID 53230361—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product3-(Trifluoromethyl)benzenepropanalHCID 11298612—

Reaction Conditions

Temperature-77.5 °C

Reaction Steps

Methyl 3-[3-(trifluoromethyl)phenyl]propanoate (5 gm) as obtained in example 2 was added to toluene (50 ml) and then cooled to −75 to −80° C. To the solution was added a solution of diisobutylaluminium hydride (4.59 gm) in n-hexane (33 ml) slowly for 1 hour 30 minutes at −75 to −80° C. The reaction mass was maintained for 1 hour at −75 to −80° C. and then added methanol (5 ml) at −75 to −80° C. The temperature of the reaction mass was raised to 0° C. and the reaction mass was poured to the chilled water (150 ml). To the reaction mass was added ethyl acetate (50 ml) and then added sodium sulfate solution (20%, 25 ml). The reaction mass was maintained for 1 hour 30 minutes at room temperature and then filtered through celite bed. The layers were separated and the aqueous layer was extracted with toluene. The combined organic layer was dried over sodium sulfate and the solvent was distilled off under reduced pressure to obtain 4.2 gm of 3-[3-(trifluoromethyl)phenyl]propionaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921606B2
Source datasetuspto-grants-2014_12
ORD IDord-fa5685e9428f40a6a7f982fca5567540
Source noteuspto-grants-2014_12