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. 2023 May 4;9(5):e15886. doi: 10.1016/j.heliyon.2023.e15886

Table 3.

Benzaldehyde derivatives conversion to isoxazole-5(4H)-ones in the existence of PDAN-Ni@Fe3O4.

Image 1
Entry Productb code Time (min) Yield %b M.P (°C)
Ref.
Observed Reported
1 Image 2 4a 60 90 140–142 140–142 [43]
2 Image 3 4 b 25 95 214–216 211–214 [43]
3 Image 4 4c 35 92 133–135 135–138 [44]
4 Image 5 4 d 40 96 140–142 139–140 [44]
5 Image 6 4e 30 96 108–110 108–109 [44]
6 Image 7 4f 25 92 265–267 267–270 [43]
7 Image 8 4 g 45 95 171–173
8 Image 9 4 h 30 93 135–137 135–136 [45]
9 Image 10 4i 40 96 174–176 175–177 [43]
10 Image 11 4j 25 92 212–214 214–216 [43]
11 Image 12 4 k 30 90 135–137 135–136 [43]
12 Image 13 4 l 60 93 241–243 242–244 [45]
13 Image 14 4 m 80 90 174–176 173–174 [46]
14 Image 15 4n 20 96 226–228 227–228 [43]
15 Image 16 4o 60 91 202–204 202–203 [43]
16 Image 17 4p 65 90 144–145 145–146 [45]
17 Image 18 4q 50 92 146–148 146–147 [43]
18 Image 19 4r 60 93 238–239 227–229 [46]
4s 30 95 88–90
4t 60 90 174–176
19 Image 20 4u 35 92 159–161 161–162 [44]
20 Image 21 4v 30 93 214–216 213–215 [44]
21 Image 22 4w 75 95 225–227 228–226 [47]
22 Image 23 80 94 211–212 212–215 [44]
23 Image 24 4 y 40 96 149–151 150–152 [44]
24 Image 25 4z 45 91 119–121 118–120 [44]
25 Image 26 4aa 35 95 130–131
26 Image 27 4 ab 30 96 162–164 168–169 [44]
27 Image 28 4ac 25 91 196–198 194–196 [47]
28 Image 29 4ad 40 90 168–170 168–170 [17]
29 Image 30 4ae 45 92 184–186
30 Image 31 4af 40 90 167–169 168–169 [47]
31 Image 32 4 ag 50 91 195–198 189–191 [47]
32 Image 33 4ah 120 Not detected
33 Image 34 4ai 120 Not detected
34 Image 35 4aj 120 Not detected
35 Image 36 4ak 120 Not detected
36 Image 37 4 al 120 Not detected

a Reaction conditions: aldehyde (1 mmol), β-ketoester (1 mmol), hydroxylamine hydrochloride (1 mmol), 5 mL water, and PDAN-Ni@Fe3O4 (0.04 g) at 50 °C.

b

Isolated yield.