2-(Dimethylamino)ethanol → HCID 67392676, compound

HRID 909823Notes

Reaction equation

HRID 909823 reaction equation
[CH3:1][N:2]([CH3:6])[CH2:3][CH2:4][OH:5].[CH3:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([B:15]([CH:17]([O:24][CH:25]([B:32]([C:34]2[CH:39]=[CH:38][C:37]([O:40][CH3:41])=[CH:36][CH:35]=2)[OH:33])[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)O)=[CH:11][CH:10]=1>C(O)C>[CH3:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([B:15]([CH:17]([O:24][CH:25]([B:32]([C:34]2[CH:35]=[CH:36][C:37]([O:40][CH3:41])=[CH:38][CH:39]=2)[O:33][CH2:4][CH2:3][N:2]([CH3:6])[CH3:1])[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[O:5][CH2:4][CH2:3][N:2]([CH3:6])[CH3:1])=[CH:11][CH:10]=1

Participants

4

Procedure

The entitled compound (51 mg) was obtained by allowing 22 mg of N,N-dimethylethanolamine to act on 85 mg of bis(4,4′-(p-methoxyphenyl-hydroxyboryl)benzyl) ether in 0.5 mL of ethanol.

Sources & evidence

ORD record
ord-67ee35445e754eb0bf98ea3e9a0487fb
Source dataset
uspto-grants-2011_09
Patent number
US08017809B2

Reaction notes

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