Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865918Generated: November 3, 2026

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

https://huagongshe.com/reaction/1865918

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 numberUS07629353B2
Source datasetuspto-grants-2009_12
ORD IDord-3d8b21ca2ccd4dc79d93f6cf975d72b0
Source noteuspto-grants-2009_12