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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987572Generated: November 1, 2026

Hydrochloric Acid → 4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)butanal

https://huagongshe.com/reaction/1987572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant4,4,4-trifluoro-N-methoxy-N-methyl-2-(2,2,2-trifluoroethyl)butanamideHCID 57356913—
SolventDichloromethaneHCID 6344—
Product4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)butanalHCID 2523173365%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 4,4,4-trifluoro-N-methoxy-N-methyl-2-(2,2,2-trifluoroethyl)-butyramide (2.67 g, 10 mmol) in CH2Cl2 (10 mL), diisobutylaluminum hydride (2.9 mL, 16 mmol) was added over 10 min at −70° C. The reaction mixture was stirred at −70° C. for 40 min, then transferred via a cannula to a flask containing 30 mL of 2N HCl at 0° C. 10 mL of conc. HCl was added and the mixture was stirred at 25° C. for 30 min. Phases were split and the aqueous phase was extracted with 5 mL of CH2Cl2. The combined organic phase was washed with brine and dried over MgSO4. NMR analysis of the solution using an internal standard indicated formation of the title product in 65% yield. The solution was used as such for further transformations.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550629B2
Source datasetuspto-grants-2009_06
ORD IDord-6ea8c2c37b3440d28c4c0263e0db16db
Source noteuspto-grants-2009_06