Water → Ethyl 3-Bromoindole-2-carboxylate
Reaction equation
[Br:1]Br.[NH:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]1[C:12]([O:14][CH2:15][CH3:16])=[O:13].O>CN(C=O)C>[Br:1][C:5]1[C:6]2[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=2)[NH:3][C:4]=1[C:12]([O:14][CH2:15][CH3:16])=[O:13]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of bromine (2.72 ml) in DMF was added dropwise over 10 mins to a solution of ethyl indole-2-carboxylate in DMF. The reaction was stirred for 30 mins, then poured into water to precipitate a pale yellow solid which was filtered off and recrystallized from ethyl acetate to give the desired starting material as white needles (10.2 g, 72%), mp 150-151°; NMR d (CDCl3) 1.44 (t, 3H), 4.45 (q, 2H), 7.22 (m, 1H), 7.38 (m, 2H), 7.66 (d, 1H), 9.27 (brs, 1H); M/z (−) 268 (M+), 266, 196, 194.
Workup
- customto precipitate a pale yellow solid which
- filtrationwas filtered off
- customrecrystallized from ethyl acetate
- customto give the
Sources & evidence
- ORD record
- ord-cd901862d5ef46a994d74331f92297cf
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06833387B1
Reaction notes
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