Benzyl Bromide → HCID 20381759, compound

HRID 1833401Notes

Reaction equation

HRID 1833401 reaction equation
[CH3:1][O:2][C:3]([C:5]1[NH:6][C:7]2[C:12]([C:13]=1[O:14][C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=1[N+:22]([O-:24])=[O:23])=[CH:11][CH:10]=[CH:9][CH:8]=2)=[O:4].[CH2:25](Br)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>C(O)C>[CH3:1][O:2][C:3]([C:5]1[N:6]([CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:7]2[C:12]([C:13]=1[O:14][C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=1[N+:22]([O-:24])=[O:23])=[CH:11][CH:10]=[CH:9][CH:8]=2)=[O:4]

Participants

4

Reactant 2

HCID 7498Benzyl BromideHCID 54297304HCID 54297304, compound

Product 1

HCID 20381759HCID 20381759, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

In the same way as described in example 5, methyl-3-[2-nitro-4-chlorophenoxy]-indole-2-carboxylate was alkylated with benzyl bromide. Analytical material was obtained by recrystallization from ethanol, mp. 120°-1°.

Sources & evidence

ORD record
ord-ecf644c23a5348449d1d37a528b753a9
Source dataset
uspto-grants-1978_01
Patent number
US04066660

Reaction notes

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