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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980874Generated: November 1, 2026

Lithium diisopropylamide → Diisopropylamine

https://huagongshe.com/reaction/980874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 56627333HCID 56627333—
SolventTetrahydrofuranHCID 8028—
ProductDiisopropylamineHCID 7912—
ProductHCID 178418348HCID 178418348—

Reaction Steps

Subsequently, 6.1 g of the 1-benzyl-3-methyl-4-piperidone-N,N-dimethylhydrazone obtained above was dissolved in 30 ml of tetrahydrofuran. The solution were added dropwise to a solution of lithium diisopropylamide in tetrahydrofuran obtained from 23 ml of methyl lithium (1.2M ether solution), 3.8 ml of diisopropylamine and 30 ml of tetrahydrofuran at -8° C. over 15 minutes and the mixture was stirred at the same temperature for 2 hours. Thereafter, the reaction mixture was cooled to -60° C. and, to the reaction mixture was added 2.4 ml of methyl iodide. The temperature was gradually raised to 0° C. in 4 hours. The reaction mixture was poured into a mixed solvent of 120 ml of dichloromethane and 40 ml of water, and the dichloromethane layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography (eluent: chloroform:methanol=20:1 V/V) to obtain 3.8 g of 1-benzyl-3,5-dimethyl-4-piperidone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04639522
Source datasetuspto-grants-1987_01
ORD IDord-fbb5f48d281e446f942aabd221abf304
Source noteuspto-grants-1987_01