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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | (2S)-2-Aminobutanamide hydrochloride | HCID 11961924 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide, (S)- | HCID 29938341 | 78.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837223 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-069dcf33376f41e393ee9a23e3492ac6 |
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| Source note | uspto-grants-1989_06 |
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