HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Formaldehyde → 4-Methoxycarbonyl-3-methyl-2-phenylthiazolidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | 2-Phenylthiazolidine-4-carboxylic acid methyl ester | HCID 14790914 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 4-Methoxycarbonyl-3-methyl-2-phenylthiazolidine | HCID 15052257 | 100% |
Reaktionsschritte
A solution of 2.23 g of 4-methoxycarbonyl-2-phenylthiazolidine in 20 m of acetonitrile was chilled to -15° C. and, after addition of 4.3 g of 35% formalin and 1.0 g of sodium cyanoborohydride, was stirred for 30 minutes. The mixture was made acidic by addition of acetic acid under chilling with ice and, after addition of water, was made alkaline by addition of potassium carbonate. The alkaline solution was extracted with ether, and the etheral extract was dried over anhydrous sodium sulfate. The extract was placed under reduced pressure to distill of the solvent. The residue was purified by silica gel column chromatography (eluent: chloroform) to give 2.37 g of 4-methoxycarbonyl-3-methyl-2-phenylthiazolidine as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05183811 |
| Quelldatensatz | uspto-grants-1993_02 |
| ORD ID | ord-d0fde7f5f32b4592968dcf896533d930 |
| Quellennotiz | uspto-grants-1993_02 |