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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811039Generated: October 29, 2026

Sodium hydride → HCID 59375018, compound

https://huagongshe.com/reaction/1811039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorobenzyl bromideHCID 68021—
Reactant4-BromoindoleHCID 676494—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59375018HCID 59375018—

Reaction Steps

A suspension of sodium hydride (60% oil dispersion, 112 mg, 2.81 mmol) in THF (12 mL) was stirred at rt and treated with a solution of 4-bromo-1H-indole (500 mg, 2.55 mmol) in THF (3 mL). After 1-2 min, the mixture was treated with 4-fluorobenzyl bromide (0.318 mL, 2.55 mmol) and the slightly cloudy solution was stirred at rt. After 20 h, the mixture was concentrated. The residue was partitioned between EtOAc and 0.1 M hydrochloric acid, and the aqueous phase was again extracted with EtOAc. The combined organic layers were washed with brine, dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 90:10 to 50:50 hexane-EtOAc) to provide 4-bromo-1-(4-fluorobenzyl)-1H-indole as a colorless oil (461.4 mg, 85% purity, 51%) contaminated by ca. 15% by weight of 4-bromo-1,3-bis(4-fluorobenzyl)-1H-indole. 1H NMR (400 MHz, chloroform-d) δ 7.28 (1 H, dd, J=7.6, 0.8 Hz), 7.19 (1 H, d, J=8.4 Hz), 7.16 (1 H, d, J=3.3 Hz), 6.94-7.09 (5 H, m), 6.60 (1 H, dd, J=3.1, 0.9 Hz), 5.28 (2 H, s). Mass spectrum m/z 304, 306 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-d93a63ced3e64cb8af68ed1a97ae115f
Source noteuspto-grants-2013_01