Reaktion #95162

ord-508bf23e577b4350af5f2931d03eb76b

Reaktionsgleichung

CCOC(=O)C(C)(C)Oc1cccc2[nH]c(C)c(-c3ccccc3)c12
2-methyl-2-[2-methyl-3-phenyl-1H-indole-4-yloxy]-propanoic acid ethylester
CCCBr
propylbromide
→
CCCn1c(C)c(-c2ccccc2)c2c(OC(C)(C)C(=O)OCC)cccc21
2-Methyl-2-[2-methyl-3-phenyl-1-propyl-1H-indole-4-yloxy]-propanoic acid ethylester

Edukte

CCOC(=O)C(C)(C)Oc1cccc2[nH]c(C)c(-c3ccccc3)c12
2-methyl-2-[2-methyl-3-phenyl-1H-indole-4-yloxy]-propanoic acid ethylester
CCCBr
propylbromide

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The above compound was prepared from 2-methyl-2-[2-methyl-3-phenyl-1H-indole-4-yloxy]-propanoic acid ethylester and propylbromide using a procedure analogous to that of Example 63.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04343811uspto-grants-1982_08