Methacrylic Acid → (3-Formyl-4-hydroxyphenyl)methyl 2-methylprop-2-enoate

HRID 1494568Notes

Reaction equation

HRID 1494568 reaction equation
Cl[CH2:2][C:3]1[CH:10]=[C:7]([CH:8]=[O:9])[C:6]([OH:11])=[CH:5][CH:4]=1.C(=O)([O-])O.[Na+].[C:17]([OH:22])(=[O:21])[C:18]([CH3:20])=[CH2:19]>CC(C)=O>[C:17]([O:22][CH2:2][C:3]1[CH:10]=[C:7]([CH:8]=[O:9])[C:6]([OH:11])=[CH:5][CH:4]=1)(=[O:21])[C:18]([CH3:20])=[CH2:19]

Participants

5

Procedure

5-Chloromethylsalicylaldehyde (34 g) (prepared by the method of Angyal et al., J. Chem. Soc. 2141, (1950)) was added to a stirred mixture of acetone (250 ml), sodium hydrogen carbonate (33.6 g), and methacrylic acid (34.4 g)

Sources & evidence

ORD record
ord-ba985160dd0047a7aca4cd490c715933
Source dataset
uspto-grants-1991_06
Patent number
US05026860

Reaction notes

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