HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904200Generated: October 25, 2026
Potassium Carbonate → (R)-N-[1-(aminocarbonyl)propyl]-4-chlorobutanamide
https://huagongshe.com/reaction/1904200
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | (2R)-2-aminobutanamide hydrochloride | HCID 16218339 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (R)-N-[1-(aminocarbonyl)propyl]-4-chlorobutanamide | HCID 54219251 | 86% |
Reaction Steps
31.1 g (0.225 mole) of ground potassium carbonate are mixed with 12.47 g (0.09 mole) of (R)-2-aminobutanamide hydrochloride in 160 ml of acetone. The reaction mixture is cooled to 0° C. and a solution of 15.23 g (0.108 mole) of 4-chlorobutyryl chloride in 25 ml of acetone 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 100 ml of anhydrous ether for 15 minutes at a temperature between 5° and 10° C. The precipitate is filtered off, washed twice with 30 ml of ether, and dried in vacuo to obtain 16 g of (R)-N-[1-(aminocarbonyl)propyl]-4-chlorobutanamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837224 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-164e41f012ba478497a0ddb77c92a2b1 |
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| Source note | uspto-grants-1989_06 |
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