Methyl iodide → HCID 86695337, compound
Reaction equation
[Br:1][C:2]1[C:10]([Br:11])=[C:9]([Br:12])[CH:8]=[C:7]2[C:3]=1[C:4]([CH3:15])([CH3:14])[C:5]([CH3:13])=[N:6]2.[I:16][CH3:17]>>[I-:16].[Br:1][C:2]1[C:10]([Br:11])=[C:9]([Br:12])[CH:8]=[C:7]2[C:3]=1[C:4]([CH3:15])([CH3:14])[C:5]([CH3:13])=[N+:6]2[CH3:17]Participants
3
Procedure
1.12 g (2.8 mmol) of 4,5,6-tribromo-2,3,3-trimethyl-3H-indole and 2 mL (32 mmol) of iodomethane were heated in a sealed tube at 30-35° C. for 24 hours. The formed precipitate was filtered, washed with small amounts of benzene and ether to yield 700 mg (47%) of 4,5,6-tribromo-1,2,3,3-tetramethyl-3H-indolium iodide. 1H-NMR (200 MHz, DMSO-d6), δ, ppm: 8.50 (1H, s, arom.), 3.99 (3H, s, NCH3), 2.77 (3H, s, CH3), 1.60 (6H, s, C(CH3)2).
Workup
- filtrationThe formed precipitate was filtered
- washwashed with small amounts of benzene and ether
Sources & evidence
- ORD record
- ord-dc5614db2d0644fa9be135c000519cd9
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08748446B2
Reaction notes
Loading…