HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 20499913, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | N-Acetyl-L-Cysteine | HCID 12035 | — |
| Reactant | HCID 13884869 | HCID 13884869 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 20499913 | HCID 20499913 | 92.1% |
Reaction Steps
A 1.63 g quantity of L-acetylcysteine was dissolved in 0.80 g of sodium hydroxide and 50 ml of a 70% aqueous solution of ethanol with ice cooling. To the solution was added 3.02 g of N-[4-(3-ethoxy-2-hydroxypropoxy)phenyl]-3-chloropropionamide. The mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated and the residue was adjusted to a pH of 3 with diluted hydrochloric acid, washed with chloroform and extracted with ethyl acetate. The ethyl acetate layer was dewatered with Glauber's salt and was concentrated. The residue was purified with acetone-ether, giving 3.95 g of N-] 4-(3-ethoxy-2-hydroxypropoxy)phenyl]-3-(2-acetylamino-2 carboxyethylthio)propionamide in a yield of 92.1 %. ##STR5##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670583 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-ffec5a991a984e5ca6d426583ba57b5f |
| Source note | uspto-grants-1987_06 |