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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370338Generated: November 1, 2026

Water → 4-Bromo-N,N-dibenzyl-2-quinolineamine

https://huagongshe.com/reaction/1370338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromoquinolin-2-amineHCID 14067419—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-N,N-dibenzyl-2-quinolineamineHCID 18511425185.2%

Reaction Steps

A solution of 2-amino-4-bromoquinoline (244 mg, 1.09 mmol) in THF (5 mL) at 0° C. was treated with NaH (96 mg, 60% dispersion in oil, 2.4 mmol), stirred for 30 min, treated with benzyl bromide (0.335 mL, 2.4 mmol), stirred at room temperature for 3 days, poured into water (30 mL), extracted with EtOAc (2×10 mL), dried (MgSO4), concentrated in vacuo, purified by chromatography [SiO2; heptane-EtOAc (10:1)] and the resulting solid recystallised (MeOH) to give the product (407 mg, 99%) as a white crystalline solid: IR νmax (Nujol)/cm−1 3059, 3020, 2955, 2925, 2854, 1609, 1592, 1542, 1498, 1455, 1426 and 1358; NMR δH (400 MHz, CDCl3) 4.89 (4H, s), 7.15 (1H, s), 7.20-7.68 (11H, m),7.56 (1H, t, J 7.0 Hz), 7.69 (1H, d, J 8.7 Hz) and 7.94 (1H, d, J 8.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583156B1
Source datasetuspto-grants-2003_06
ORD IDord-239c4d52696947ce9944ae9066d05d90
Source noteuspto-grants-2003_06