HCID 57913426, compound → HCID 57913428, compound
Reaction equation
ClC1C=CC([C:8]([C:36]2[CH:41]=[CH:40][C:39]([Cl:42])=[CH:38][CH:37]=2)(OC)[C:9]2[CH:14]=[C:13]([OH:15])[C:12]([C:16](C3C=CC(Cl)=CC=3)([C:19]3[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=3)OC)=[CH:11][C:10]=2[OH:33])=CC=1>[N+](C1C=CC=CC=1)([O-])=O>[Cl:25][C:22]1[CH:23]=[CH:24][C:19]2[C:16]([C:36]3[CH:37]=[CH:38][C:39]([Cl:42])=[CH:40][CH:41]=3)=[C:12]3[C:13](=[CH:14][C:9]4[C:10]([O:33][C:24]5[C:19]([C:8]=4[C:36]4[CH:41]=[CH:40][C:39]([Cl:42])=[CH:38][CH:37]=4)=[CH:20][CH:21]=[C:22]([Cl:25])[CH:23]=5)=[CH:11]3)[O:15][C:20]=2[CH:21]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the product from example a (2,5-bis-[bis-(4-chloro-phenyl)-methoxy-methyl]-benzene-1,4-diol, 1.0 g, 1.56 mmol) is dissolved in nitrobenzene (5 ml) and the solution heated at reflux. The initially colourless solution turns red and later deeply violet. After one hour at reflux, the mixture is allowed to cool and then filtered. The product (violet needles) is washed with plenty of methanol and dried. MS shows the correct mass and isotopic pattern of four chlorines.
Workup
- temperaturethe solution heated
- temperatureat reflux
- temperatureAfter one hour at reflux
- temperatureto cool
- filtrationfiltered
- washThe product (violet needles) is washed with plenty of methanol
- customdried
Sources & evidence
- ORD record
- ord-4127c95d3fe44494b45401b72239d756
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08471019B2
Reaction notes
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