Epichlorohydrin → HCID 58097195, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:6][C:7]3[C:12]([C:13]=2[CH:14]=1)=[CH:11][C:10]([CH3:15])=[CH:9][CH:8]=3.[CH2:16]([CH:18]1[O:20][CH2:19]1)Cl>>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH2:16][CH:18]3[CH2:19][O:20]3)[C:7]3[C:12]([C:13]=2[CH:14]=1)=[CH:11][C:10]([CH3:15])=[CH:9][CH:8]=3Participants
3
Procedure
Following Representative Procedure 1, 3,6-dimethyl carbazole (Beyer, M.; Fritscher, J.; Feresin, E.; Schiemann, O. J. Org. Chem. 2003, 68, 2209-2215) was added to epichlorohydrin in 69% yield.
Sources & evidence
- ORD record
- ord-4ca06d143aae4eb89364fb5a67fa5016
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08604074B2
Reaction notes
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