HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-methyl-N-propionyl-L-alanine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propionic anhydride | HCID 31263 | — |
| Reactant | N-Methyl-L-alanine methyl ester hydrochloride (1:1) | HCID 13850987 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-methyl-N-propionyl-L-alanine methyl ester | HCID 53825128 | — |
Reaction Steps
In 150 ml of chloroform was dissolved 28 g (0.18 mol) of N-methyl-L-alanine methyl ester hydrochloride, followed by addition of 27 g (0.21 mol) of propionic anhydride and 33 ml of triethylamine. The mixture was allowed to stand at room temperature overnight. With the addition of 100 ml of water, the reaction mixture was stirred at room temperature for 30 minutes. Thereafter, 600 ml of ethyl acetate was added and the organic layer was washed with aqueous sodium hydrogen carbonate and water in the order mentioned, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. In the above manner, N-methyl-N-propionyl-L-alanine methyl ester was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04190580 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-9012666e60ed4a81a3cd3be2de419d0d |
| Source note | uspto-grants-1980_02 |