Piconol → HCID 67393193, compound

HRID 909828Notes

Reaction equation

HRID 909828 reaction equation
[C:1]1([B:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[B:22]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[OH:23])[OH:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O[CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][N:33]=1>C(O)C>[C:1]1([B:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[B:22]([C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=2)[O:23][CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][N:33]=2)[O:8][CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][N:33]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

4

Reactant 2

HCID 11474PiconolHCID 67392250HCID 67392250, compound

Product 1

HCID 67393193HCID 67393193, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The entitled compound (38 mg) was obtained by allowing 42 mg of bis(4,4′-(phenylhydroxyboryl)phenyl) ether and 20 mg of 2-hydroxymethylpyridine to act in 0.25 mL of ethanol.

Sources & evidence

ORD record
ord-f253b002d29e46d4812cc3802d1045b3
Source dataset
uspto-grants-2011_09
Patent number
US08017809B2

Reaction notes

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