HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → N-Acetyl-S-methyl-L-cysteine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | (-)-S-Methyl-L-cysteine | HCID 24417 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Produkt | N-Acetyl-S-methyl-L-cysteine | HCID 13893975 | 89,7% |
Reaktionsschritte
A solution of 13.5 g (100 mmole) of S-methyl-L-cysteine dissolved in 210 ml of 1 N sodium hydroxide solution was ice cooled and 10.4 ml (110 mmole) of acetic anhydride was added thereto dropwise. After 2.0 hours at room temperature, the mixture was acidified to pH 1.0 with 6 N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated in vacuo to give 15.9 g (89.6% yield) of S-methyl-N-acetyl-L-cysteine as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04440788 |
| Quelldatensatz | uspto-grants-1984_04 |
| ORD ID | ord-1289b227d0be43a18e1a3d5cb961e5a3 |
| Quellennotiz | uspto-grants-1984_04 |