HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Thiophene → methyl N-(2,3-dihydro-3-methyl-1H-inden-1-yl)glycine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Thiophene | HCID 8030 | — |
| Edukt | Glycine methyl ester | HCID 69221 | — |
| Edukt | 3-Methyl-indan-1-one | HCID 259560 | — |
| Edukt | Sodium Formate | HCID 2723810 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | methyl N-(2,3-dihydro-3-methyl-1H-inden-1-yl)glycine | HCID 67861921 | 54,1% |
Reaktionsschritte
A mixture of 21 parts of 2,3-dihydro-3-methyl-1H-inden-1-one, 25 parts of methyl 2-aminoacetate, 2 parts of a solution of thiophene in methanol 4%, 25 parts of sodium formate and 480 parts of methanol is hydrogenated in a Parr-apparatus and at 50° C. with 5 parts of palladium-on-charcoal catalyst 10%. The reaction mixture is evaporated. The residue is taken up in water and 1,1'-oxybisethane is added. The separated organic layer is extracted with a hydrochloric acid solution 10%. The aqueous layer is made alkaline and the product is extracted with 1,1'-oxybisethane. The combined extracts are dried, filtered and evaporated, yielding 19 parts (54.1%) of methyl N-(2,3-dihydro-3-methyl-1H-inden-1-yl)glycine as a residue.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05246915 |
| Quelldatensatz | uspto-grants-1993_09 |
| ORD ID | ord-e1764cad45a24269bfb95b0d00a282b2 |
| Quellennotiz | uspto-grants-1993_09 |