Acrylonitrile → HCID 54152861, compound
Reaction equation
[C:1]([CH2:3][CH2:4][O:5]CCOC(O)C)#N.[C:12](#[N:15])[CH:13]=[CH2:14].[CH2:16]([OH:22])[CH2:17][O:18][CH2:19][CH2:20][OH:21]>>[C:4]([O:22][CH2:16][CH2:17][O:18][CH2:19][CH2:20][O:21][CH2:14][CH2:13][C:12]#[N:15])(=[O:5])[CH:3]=[CH2:1]Participants
4
Procedure
Following the procedures described in Example 1, cyanoethoxyethoxyethanol (bp 144°-151° C./2 mm Hg) is prepared from diethylene glycol and acrylonitrile, acrylation of which gives the desired product.
Sources & evidence
- ORD record
- ord-d05174291e5f4040828aedd67014bbe7
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04333963
Reaction notes
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