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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904198Generated: October 25, 2026

Potassium Carbonate → N-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide, (S)-

https://huagongshe.com/reaction/1904198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant(2S)-2-Aminobutanamide hydrochlorideHCID 11961924—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductN-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide, (S)-HCID 2993834178.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

345.6 g (2.5 moles) of ground potassium carbonate are mixed with 138.5 g (1 mole) of (S)-2-amino-butanamide hydrochloride in 2.5 liters of acetonitrile. The reaction mixture is cooled to 0° C. and a solution of 129.2 g (1.2 mole) of 4-chlorobutyryl chloride in 500 ml of acetonitrile is introduced dropwise. After the addition, the reaction mixture is allowed to return to ambient temperature; the insoluble matter is filtered off and the filtrate evaporated under reduced pressure. The crude residue obtained is stirred in 1.2 liter of anhydrous ether for 30 minutes at a temperature between 5° and 10° C. The precipitate is filtered off, washed twice with 225 ml of ether and dried in vacuo to obtain 162.7 g of (S)-N-[1-(aminocarbonyl)propyl]-4-chlorobutanamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837223
Source datasetuspto-grants-1989_06
ORD IDord-069dcf33376f41e393ee9a23e3492ac6
Source noteuspto-grants-1989_06