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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716416Generated: November 2, 2026

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

https://huagongshe.com/reaction/1716416

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 bromide 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 numberUS07803815B2
Source datasetuspto-grants-2010_09
ORD IDord-7737022d17cb4f4f9f017a48d4ace947
Source noteuspto-grants-2010_09