HCID 86747918, compound → HCID 22598642, compound

HRID 1109678Notes

Reaction equation

HRID 1109678 reaction equation
[N+:1]([C:4]1[CH:45]=[C:44]([CH3:46])[C:7]([O:8][C:9]2[CH:43]=[CH:42][C:12]([C:13]([C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([C:22]([CH3:41])([CH3:40])[C:23]4[CH:28]=[CH:27][C:26]([O:29][C:30]5[C:35]([CH3:36])=[CH:34][C:33]([N+:37]([O-])=O)=[CH:32][CH:31]=5)=[CH:25][CH:24]=4)[CH:17]=3)([CH3:15])[CH3:14])=[CH:11][CH:10]=2)=[CH:6][CH:5]=1)([O-])=O.[H][H]>[Pd].C(O)(C)C>[NH2:37][C:33]1[CH:34]=[C:35]([CH3:36])[C:30]([O:29][C:26]2[CH:25]=[CH:24][C:23]([C:22]([C:18]3[CH:19]=[CH:20][CH:21]=[C:16]([C:13]([CH3:15])([CH3:14])[C:12]4[CH:42]=[CH:43][C:9]([O:8][C:7]5[C:44]([CH3:46])=[CH:45][C:4]([NH2:1])=[CH:5][CH:6]=5)=[CH:10][CH:11]=4)[CH:17]=3)([CH3:41])[CH3:40])=[CH:28][CH:27]=2)=[CH:31][CH:32]=1

Participants

5

Procedure

Successively, to a reduction vessel equipped with a thermometer, reflux condenser and stirrer, 120 g (0.195 mol) of 1,3-bis[4-(4-nitro-6-methylphenoxy)-α, α-dimethylbenzyl]benzene, 400 g of isopropyl alcohol and 5 g of 5%-Pd/c having a moisture content of 50% were charged and reacted at 70°~80° C. for 4 hours in a hydrogen atmosphere. After finishing the reaction, the catalyst was filtered off and the filtrate was concentrated under reduced pressure to obtain 89.0 g (82% yield) of 1,3-bis[4-(4-amino-6-methylphenoxy)-α, α-dimethylbenzyl]benzene as a light yellow crystal having a melting point of 118.1~118.2.

Workup

  1. customSuccessively, to a reduction vessel equipped with a thermometer
  2. temperaturereflux condenser and stirrer
  3. additionwere charged
  4. customthe reaction
  5. filtrationthe catalyst was filtered off
  6. concentrationthe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-9c357128c81741239dd8b201443492db
Source dataset
uspto-grants-1994_06
Patent number
US05321096

Reaction notes

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