Reaktion #1622045

ord-e3c5aef6dbaf467e9cf53cade32cdb9f

Reaktionsgleichung

CCOC(=O)C(Cl)=NNc1ccc(Cl)cc1
compound
CCOC(=O)C(Cl)=NNc1ccc(Cl)cc1
Ethyl chloro[2-(4-chlorophenyl)hydrazono]acetate
C=C(C)c1ccc(Cl)cc1
4-chloro-α-methyl styrene
CCOC(=O)C1=NN(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)C1
title compound
CCOC(=O)C1=NN(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)C1
Ethyl 1,5-bis(4-Chlorophenyl)-4,5-dihydro-5-methyl-1H-pyrazole-3-carboxylate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The compound of Example 6 (1.0 gm) was converted to the title compound (0.6 gm) by adaptation of the procedure of Example 9 to 4-chloro-α-methyl styrene (2.5 ml). The product was a yellow oil. NMR (CDCl3) 7.3-6.8 (m, ArH, 8H), 4.3 (q, 2H, CH2), 3.3 (m, 2H, CH2), 1.8 (s, 3H, CH3), 1.3 (t, 3H, CH3).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05091405uspto-grants-1992_02