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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221217Generated: November 2, 2026

Benzyl Bromide → HCID 10613176, compound

https://huagongshe.com/reaction/2221217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant7-BromoindoleHCID 2757020—
SolventDimethylformamideHCID 6228—
ProductHCID 10613176HCID 10613176—

Reaction Steps

1-Benzyl-7-bromo-1H-indole was prepared from 7-bromo-1H-indole (0.500 g, 2.55 mmol), sodium hydride (0.285 g, 7.13 mmol of 60% dispersion on mineral oil), benzyl bromide (0.67 mL, 5.6 mmol) in DMF (5 mL). The reaction mixture was stirred for 1 hour after the addition of sodium hydride and for 1 hour after the addition of benzyl bromide. The compound was purified by flash chromatography (using hexane as an eluant) and dried at 60° C. for 30 minutes to yield a cream-colored solid (0.508 g, 70%), mp: 74-75° C. 1HNMR (300 MHz, DMSO-d6): δ 7.5-7.65 (m, 2H), 7.15-7.35 (m, 4H), 6.8-7.0 (m, 3H), 6.6 (s, 1H), and 5.8 ppm (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368471B2
Source datasetuspto-grants-2008_05
ORD IDord-9ef8c67f1c504892a365bb8197427474
Source noteuspto-grants-2008_05