Acrylic Acid → HCID 22759780, compound

HRID 1703757Notes

Reaction equation

HRID 1703757 reaction equation
[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([N:20]1[C:26]([CH3:28])([CH3:27])[C:24](=[O:25])[N:23]([CH2:29][CH:30]2[O:32][CH2:31]2)[C:21]1=[O:22])[N:7]1[C:13]([CH3:15])([CH3:14])[C:11](=[O:12])[N:10]([CH2:16][CH:17]2[O:19][CH2:18]2)[C:8]1=[O:9]>>[CH2:6]([N:20]1[C:26]([CH3:27])([CH3:28])[C:24](=[O:25])[N:23]([CH2:29][CH:30]([OH:32])[CH2:31][O:5][C:1](=[O:4])[CH:2]=[CH2:3])[C:21]1=[O:22])[N:7]1[C:13]([CH3:14])([CH3:15])[C:11](=[O:12])[N:10]([CH2:16][CH:17]([OH:19])[CH2:18][O:4][C:1](=[O:5])[CH:2]=[CH2:3])[C:8]1=[O:9]

Participants

3

Procedure

1,1'-Methylene-bis[3-(3-acryloyloxy-2-hydroxypropyl)-5,5-dimethylhydantoin] is prepared by the reaction of acrylic acid and 1,1'-methylene-bis[3-glycidyl-5,5-dimethylhydantoin], see preparation in Example 3b, according to Example 1 of U.S. Pat. No. 3,808,226.

Workup

  1. custompreparation in Example 3b

Sources & evidence

ORD record
ord-2053c0723e644500bc58732f3ea1efb1
Source dataset
uspto-grants-1978_11
Patent number
US04125516

Reaction notes

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