Epichlorohydrin → HCID 10357090, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[O:10][CH:9]=[C:8]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:7]2=[O:18].[CH2:19]([CH:21]1[O:23][CH2:22]1)Cl>CC(O)C>[O:23]1[CH2:22][CH:21]1[CH2:19][O:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[O:10][CH:9]=[C:8]([C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)[C:7]2=[O:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the procedure of Example 1a, the title compound was prepared from the reaction of 8-hydroxyisoflavone with epichlorohydrin, mp 141°-143° C. (i-PrOH).
Sources & evidence
- ORD record
- ord-09d5e0230bfb4d379b0172520f874f4d
- Source dataset
- uspto-grants-1989_12
- Patent number
- US04889941
Reaction notes
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