Methyl Acrylate → HCID 20318456, compound
Reaction equation
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[C:4]([C:9]([CH3:16])([CH3:15])[CH2:10][C:11]([CH3:14])([CH3:13])[CH3:12])[C:3]=1[OH:17].[C:18]([O:22][CH3:23])(=[O:21])[CH:19]=[CH2:20]>>[CH3:8][C:7]1[C:2]([CH3:1])=[C:3]([OH:17])[C:4]([C:9]([CH2:10][C:11]([CH3:12])([CH3:14])[CH3:13])([CH3:16])[CH3:15])=[CH:5][C:6]=1[CH2:20][CH2:19][C:18]([O:22][CH3:23])=[O:21]Participants
3
Procedure
The product was obtained by reacting 2,3-dimethyl-6-(1,1,3,3-tetramethylbutyl)phenol with methyl acrylate in a similar manner as described in Example 1. The desired product was obtained as white crystals melting at 83° to 85° C (Compound 2).
Workup
- customThe product was obtained
Sources & evidence
- ORD record
- ord-749a560d921f4c999420370dea8c2d67
- Source dataset
- uspto-grants-1978_07
- Patent number
- US04101550
Reaction notes
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