HCID 15114139, compound → HCID 15114140, compound
Reaction equation
[CH2:1]([O:11][C:12]1[CH:13]=[C:14]2[C:19](=[CH:20][CH:21]=1)[CH:18]=[C:17]([CH2:22][OH:23])[CH:16]=[CH:15]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH2:1]([O:11][C:12]1[CH:13]=[C:14]2[C:19](=[CH:20][CH:21]=1)[CH:18]=[C:17]([CH:22]=[O:23])[CH:16]=[CH:15]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
In 10 ml of chloroform, 84 mg (0.43 mmol) of the thus obtained 6-decyloxy-2-hydroxymethylnaphthalene was dissolved, and 235 mg (2.57 mmol) of activated manganese dioxide powder was added. The oxidation reaction was carried out with vigorous stirring at room temperature for 12 hours.
Workup
- customThe oxidation reaction
Sources & evidence
- ORD record
- ord-331fa00e8b004edf98ea4ef3a4378078
- Source dataset
- uspto-grants-1992_09
- Patent number
- US05143644
Reaction notes
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