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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836469Generated: October 30, 2026

Benzyl Bromide → HCID 74057329, compound

https://huagongshe.com/reaction/1836469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant5331-92-0HCID 220741—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 74057329HCID 7405732967%

Reaction Conditions

Temperature22 °C

Reaction Steps

Sodium hydride (1.05 g of 60% suspension in mineral oil, 0.63 g, 26.3 mmol) was washed with hexane, suspended in tetrahydrofuran (10 ml) and then treated with benzyl bromide (2.7 ml, 22.8 mmol) A solution of the above oxime in tetrahydrofuran (10 ml) was then added dropwise and the resulting mixture was stirred at 22° C. for 18 h. The reaction mixture was then diluted with dichloromethane, washed with water, brine and dried. Evaporation of the solvent and chromatography of the residue on silica gel (elution hexane-toluene, 8:2 to 1:1) gave 4.30 g (67% yield) of the title oxime ether as a clear oil. 1HNMR 400 MHz (CDCl3) δ (ppm): 5.12 (2H, s, OCH2), 7.3-7.44 (7H, m, aromatics), 7.68 (1H, d, aromatic), 8.04 (1H, s, CH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777440B2
Source datasetuspto-grants-2004_08
ORD IDord-f62080dea45847469f01ccb40a461a2b
Source noteuspto-grants-2004_08