HCID 86739679, compound → HCID 20442911, compound

HRID 1632476Notes

Reaction equation

HRID 1632476 reaction equation
[CH3:1]/[C:2](=[CH:6]\[CH:7]=[CH:8]\[C:9](\[CH3:26])=[CH:10]\[CH2:11][C:12]1[C:17]([Cl:18])=[CH:16][C:15]([O:19][C:20]([F:23])([F:22])[F:21])=[C:14]([CH3:24])[C:13]=1[Cl:25])/[CH:3]=[CH:4]/[OH:5]>[O-2].[O-2].[Mn+4].C(Cl)Cl>[CH3:1]/[C:2](/[CH:6]=[CH:7]/[CH:8]=[C:9](\[CH3:26])/[CH:10]=[CH:11]/[C:12]1[C:17]([Cl:18])=[CH:16][C:15]([O:19][C:20]([F:22])([F:21])[F:23])=[C:14]([CH3:24])[C:13]=1[Cl:25])=[CH:3]\[CH:4]=[O:5]

Participants

4

Procedure

(2E,4E,6E,8E)-3,7-dimethyl-9-[2,6-dichloro-3methyl-4-(trifluoromethoxy)phenyl]-nonatetraen-1-ol (0.6mmol) could be dissolved in 20 ml. of methylene chloride and added to a suspension of 1.1 g. of activated manganese dioxide in 40 ml. of methylene chloride with stirring. Ater the reaction is complete, the resulting mixture is filtered and the filtrate evaporated to give (2E,4E,6E,8E)-3,7-dimethyl-9-[2,6-dichloro-3-methyl-4-(trifluoromethoxy)phenyl]-nonatetraen-1-al, which is further purified by crystallization or chromatography using conventional procedures.

Workup

  1. filtrationthe resulting mixture is filtered
  2. customthe filtrate evaporated

Sources & evidence

ORD record
ord-2bb5e34b9fed477093c525f1941c9669
Source dataset
uspto-grants-1984_10
Patent number
US04476056

Reaction notes

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