HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Acetyl-L-Cysteine → HCID 57291887, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Acetyl-L-Cysteine | HCID 12035 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 4-Bromobutyric acid | HCID 75809 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57291887 | HCID 57291887 | — |
Reaction Steps
A solution of 4-bromobutyric acid (5.1 g, 30.6 mmoles) and 1,1′-carbonyldiimidazol (5.61 g, 34.6 mmoles)) in chloroform (50 ml) is left at room temperature under stirring for 1 hour. To the reaction mixture N-acetyl cysteine (5 g, 30.6 mmoles) dissolved in N,N-dimethylformamide (5 ml) and sodium ethylate (50 mg) is added under stirring. After 24 hours the solution is washed with HCl 1% and brine, the organic phase is anhydrified with sodium sulphate and evaporated at reduced pressure. The obtained crude product is purified by chromatography on silica gel column, eluting with ethyl acetate/chloroform 7/3. N-acetyl-S-(4-bromobutyroyl)cysteineis obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524836B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-d96d278ce85f4bddb7821bcc502d6938 |
| Source note | uspto-grants-2009_04 |