HCID 22564193, compound → HCID 22564192, compound

HRID 982917Notes

Reaction equation

HRID 982917 reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:10]3[C:15]([C:16]([C:23]4[CH:28]=[CH:27][C:26]([O:29]C)=[C:25]([N+:31]([O-:33])=[O:32])[CH:24]=4)=[C:17]4[C:22]=2[CH:21]=[CH:20][CH:19]=[CH:18]4)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:5][C:4]=1[N+:34]([O-:36])=[O:35]>CC(=O)CC.Br>[OH:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:22]3[C:17]([C:16]([C:23]4[CH:28]=[CH:27][C:26]([OH:29])=[C:25]([N+:31]([O-:33])=[O:32])[CH:24]=4)=[C:15]4[C:10]=2[CH:11]=[CH:12][CH:13]=[CH:14]4)=[CH:18][CH:19]=[CH:20][CH:21]=3)=[CH:5][C:4]=1[N+:34]([O-:36])=[O:35]

Participants

4

Procedure

19.2 g (0.04 mol) of 9,10-bis(4-methoxy-3-nitrophenyl)-anthracene in a mixture of 200 ml of butanone and 200 ml of concentrated HBr are refluxed for 24 h while stirring. After the end of the reaction, the suspension is evaporated down to half its volume in a rotary evaporator and the product is filtered off with suction. Recrystallization from toluene is then effected.

Workup

  1. temperatureare refluxed for 24 h
  2. customAfter the end of the reaction
  3. customthe suspension is evaporated down to half its volume in a rotary evaporator
  4. filtrationthe product is filtered off with suction
  5. customRecrystallization from toluene

Sources & evidence

ORD record
ord-38d709a5f31245fd9f4a8a5c34b50364
Source dataset
uspto-grants-2005_03
Patent number
US06861560B2

Reaction notes

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