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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5779Erstellt: 23. Oktober 2026

Thiophene → methyl N-(2,3-dihydro-3-methyl-1H-inden-1-yl)glycine

https://huagongshe.com/de/reaction/5779

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiopheneHCID 8030—
EduktGlycine methyl esterHCID 69221—
Edukt3-Methyl-indan-1-oneHCID 259560—
EduktSodium FormateHCID 2723810—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produktmethyl N-(2,3-dihydro-3-methyl-1H-inden-1-yl)glycineHCID 6786192154,1%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05246915
Quelldatensatzuspto-grants-1993_09
ORD IDord-e1764cad45a24269bfb95b0d00a282b2
Quellennotizuspto-grants-1993_09