Methacrylic Acid → HCID 86707575, compound
Reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[C:15]([OH:17])[CH:14]=[C:13]([C:18]3[CH:23]=[CH:22][C:21]([CH2:24][CH2:25][CH2:26][OH:27])=[CH:20][CH:19]=3)[CH:12]=2)=[CH:7][CH:6]=1.[C:28]([OH:33])(=O)[C:29]([CH3:31])=[CH2:30]>>[CH3:30][C:29](=[CH2:31])[C:28]([O:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:6]=[CH:7][C:8]([C:11]2[CH:16]=[C:15]([O:17][C:28](=[O:33])[C:29]([CH3:31])=[CH2:30])[CH:14]=[C:13]([C:18]3[CH:23]=[CH:22][C:21]([CH2:24][CH2:25][CH2:26][O:27][C:28](=[O:33])[C:29]([CH3:31])=[CH2:30])=[CH:20][CH:19]=3)[CH:12]=2)=[CH:9][CH:10]=1)=[O:33]Participants
3
Procedure
In analogy to step 2 of example 1, 4,4″-bis-(3-hydroxy-propyl)-[1,1′;3′,1″]terphenyl-5′-ol and methacrylic acid are reacted to give 2-methyl-acrylic acid-4,4″-bis-[3-(2-methyl-acryloyloxy)-propyl]-[1,1′;3′,1″]terphenyl-5′-yl ester as colourless oil.
Sources & evidence
- ORD record
- ord-fbb01878ef9742128443b6bda4865e49
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133395B2
Reaction notes
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