Methyl iodide → 1,3-Benzodioxol-5-amine, N-methyl-
Reaction equation
[CH2:1]1[O:10][C:9]2[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=2[O:2]1.I[CH3:12]>>[CH3:12][NH:6][C:5]1[CH:7]=[CH:8][C:9]2[O:10][CH2:1][O:2][C:3]=2[CH:4]=1Participants
3
Procedure
The title compound was prepared from 3,4-(methylenedioxy)aniline and iodomethane by the procedure described in example 2 in 18% yield. 1H NMR (CDCl3): 6.67 (d, J=8.3, 1H), 6.25 (d, J=2.2, 1H), 6.04 (dd, J=2.2, 8.3, 1H), 5.85 (s, 2H), 3.50 (br s, 1H), 2.79 (s, 3H).
Sources & evidence
- ORD record
- ord-aa378083990849f0b32187b076a83abd
- Source dataset
- uspto-grants-2004_07
- Patent number
- US06765006B2
Reaction notes
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