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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099511Generated: October 25, 2026

Ethyl acetate hexane → (S)-2-(dibenzylamino)pentanal

https://huagongshe.com/reaction/1099511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl acetate hexaneHCID 21226206—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant(S)-2-(dibenzylamino)-N-methoxy-N-methylpentanamideHCID 44223340—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(dibenzylamino)pentanalHCID 4422334194.3%

Reaction Steps

To anhydrous tetrahydrofuran (1.5 L) previously cooled to −20° C. to −30° C. was added solid lithium aluminum hydride (33.5 g; 0.882 mol; 120 mole %) slowly with stirring. A solution of (S)-2-(dibenzylamino)-N-methoxy-N-methylpentanamide (6) (250 g; 0.735 mol) in anhydrous tetrahydrofuran (1 L) at −30° C. was slowly added to the above mixture under a nitrogen atmosphere. The reaction was continued for 2 hours at −30° C., monitoring progress of the reaction by TLC analysis (ethyl acetate/hexane, 1:9). Upon completion of the reaction, the excess reagent was quenched by the dropwise addition of ethyl acetate (1 L) and ice-cold water (300 ml) at −30° C. The insoluble salts were filtered through celite, the filtrate diluted with water (3 L), and the product extracted into ethyl acetate (2 L). The combined ethyl acetate layers were washed with water (2 L), dried over sodium sulfate, filtered, and solvent removed under reduced pressure to provide (S)-2-(dibenzylamino)pentanal (7) (195 g) as a light yellow oil, which was used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143448B2
Source datasetuspto-grants-2012_03
ORD IDord-89d798f1f0da431db63a6db371f79aba
Source noteuspto-grants-2012_03