HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
L-Methionine → N(4-aminobenzoyl)-L-methionine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | L-Methionine | HCID 6137 | — |
| Edukt | Benzoyl chloride, 4-amino- | HCID 177720 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | N(4-aminobenzoyl)-L-methionine | HCID 22851148 | — |
Reaktionsschritte
In an Erlenmeyer flask, 1.35 g of para-aminobenzoic acid chloride are dissolved in 20 ml benzene in the presence of 2.8 ml triethylamine. 1.49 g L-methionine is added progressively and the resultant mixture is filtered. After evaporation of the filtrate to dryness under vacuum (15 mm Hg), the residue is dissolved in N hydrochloric acid and extracted with chloroform. The chloroformic solution is successively washed with several ml of 10% aqueous HKCO3 solution and with water. It is then collected, dried over magnesium sulfate and evaporated. The product obtained is precipitated in cyclohexane and filtered. After recrystallization in a (1:1) mixture of 95 alcohol-water, 1.95 g of white crystals are isolated. M.p.: 172° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05298647 |
| Quelldatensatz | uspto-grants-1994_03 |
| ORD ID | ord-197240ff4471474cbc02312e932c5995 |
| Quellennotiz | uspto-grants-1994_03 |