反应 #455509

ord-e07743831d6747b48904e6ed628280d2

反应方程式

Cl.O=C1CCCc2cc(OCCc3c[nH]cn3)ccc21
6-[2-(1H-imidazole-4-yl)-ethoxy]-3,4-dihydro-2H-naphthalen-1-one, monohydrochloride
Cc1ccc(C=O)s1
5-methyl-2-thiophene carboxaldehyde
Cc1ccc(C=C2CCc3cc(OCCc4c[nH]cn4)ccc3C2=O)s1
title compound
收率 53.1%
Cc1ccc(C=C2CCc3cc(OCCc4c[nH]cn4)ccc3C2=O)s1
6-[2-(1H-Imidazole-4-yl)-ethoxy]-2-(5-methyl-thiophen-2-ylmethylene)-3,4-dihydro-2H-naphthalen-1-one
收率 53.1%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

According to the method of Example 34, 6-[2-(1H-imidazole-4-yl)-ethoxy]-3,4-dihydro-2H-naphthalen-1-one, monohydrochloride (0.313 g, 1.07 mmol) was reacted with 5-methyl-2-thiophene carboxaldehyde (0.142 g, 1.13 mmol) in 5 mL of 4% KOH in EtOH overnight to afford 0.207 g (44%) of the title compound as a bright orange solid, mp 69-70° C.: CI-MS m/e 364 (M+), 365 (M+ +1).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06133303uspto-grants-2000_10