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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055437Generated: November 1, 2026

Benzyl Bromide → 1-benzyl-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/2055437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantIndole-3-Carboxylic AcidHCID 69867—
SolventDimethylformamideHCID 6228—
Product1-benzyl-1H-indole-3-carboxylic acidHCID 3367178.3%

Reaction Steps

To a stirred solution of 0.50 g (3.10 mmol) 1H-indole-3-carboxylic acid 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 0.61 g (78%) of 1-benzyl-1H-indole-3-carboxylic acid as a white solid. ES-MS m/e (%): 250 (M−H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332501B2
Source datasetuspto-grants-2008_02
ORD IDord-5c37c86c43a949118ccd7bdaf91d8d35
Source noteuspto-grants-2008_02