N-(2-Hydroxyethyl)aniline → Bis(4,4'-(phenyl-phenylaminoethoxyboryl)benzyl) ether
Reaction equation
[C:1]1([B:7]([CH:9]([O:16][CH:17]([B:24]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[OH:25])[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[OH:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:32]1([NH:38][CH2:39][CH2:40]O)[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>C(O)C>[C:1]1([B:7]([CH:9]([O:16][CH:17]([B:24]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[O:25][CH2:40][CH2:39][NH:38][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[O:8][CH2:40][CH2:39][NH:38][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The entitled compound (43 mg) was obtained by allowing 40.6 mg of bis(4,4′-(phenylhydroxyboryl)benzyl) ether and 14 mg of phenylglycinol to act in 1 mL of ethanol.
Sources & evidence
- ORD record
- ord-3a3934d1e4954577938127ae68982292
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08017809B2
Reaction notes
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