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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055436Generated: November 1, 2026

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

https://huagongshe.com/reaction/2055436

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 numberUS07332501B2
Source datasetuspto-grants-2008_02
ORD IDord-ea1070e329aa4d7a8f74396ba973e126
Source noteuspto-grants-2008_02