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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865917Generated: November 3, 2026

Benzyl Bromide → 1-Benzyl-2-methyl-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1865917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-Methyl-1H-indole-3-carboxylic acidHCID 3159671—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-2-methyl-1H-indole-3-carboxylic acidHCID 66743481—

Reaction Steps

To a stirred solution of 0.50 g (3.10 mmol) 2-methyl-1H-indole-3-carboxylic acid (described in J. Heterocyclic Chem. 1977, 14, 1123) in 5 ml DMF was added 0.27 g (6.75 mmol) of NaH (60% in oil). The mixture was stirred at RT for 30 min. and then 0.39 ml (3.28 mmol) of benzyl bromid was added. The mixture was stirred an additional hour and then poured onto water and extracted with ethyl acetate. The combined organic phases were dried over Na2SO4 and concentrated in vacuo. Crystallization in Et2O afforded 1-Benzyl-2-methyl-1H-indole-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629353B2
Source datasetuspto-grants-2009_12
ORD IDord-8ca8254a529b4f8ca6c90968ae563c40
Source noteuspto-grants-2009_12