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. 2025 Sep 30;15(43):36237–36248. doi: 10.1039/d5ra03505h

Table 2. Optimization of reaction conditions for aerobic dehydrogenation of 2-phenyl-2,3 dihydroquinazolin-4(1H)-one using CuMnFe-LDHzyme/mediator catalytic systema.

Entry Mediator (mol%) Amount of CuMnFe-LDHzyme Temperature(°C) Solvent Yield (%)
1 DDQ (5) 140 60 CH3CN 72
2 4-Phenyl urazole(5) 140 60 CH3CN 70
3 DDQ (10) 140 60 CH 3 CN 98 b
4 4-Phenyl urazole(10) 140 60 CH 3 CN 98 b
5 DDQ (10) 110 60 CH3CN 68
6 4-Phenyl urazole (10) 110 60 CH3CN 65
7 DDQ (10) 130 60 CH3CN 85
8 4-Phenyl urazole(10) 130 60 CH3CN 80
9 DDQ (10) 140 45 CH3CN 70
10 4-Phenyl urazole(10) 140 45 CH3CN 75
11 DDQ (10) 140 60 CH3CN/H2O 35
12 4-Phenyl urazole(10) 140 60 CH3CN/H2O 30
13 DDQ (10) 140 60 DMSO 60
14 4-Phenyl urazole(10) 140 60 DMSO 60
a

Reaction conditions unless stated otherwise: substrate (1 mmol), CuMnFe-LDHzyme (140 mg), mediator (10 mol%), solvent (3 mL) under O2 (balloon), and 18 h;

b

The bolds represent the effective reaction conditions.