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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425018Generated: October 28, 2026

Benzyl Bromide → 1-(3-Nitro-4-phenylmethoxyphenyl)ethanone

https://huagongshe.com/reaction/2425018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxy-3-NitroacetophenoneHCID 138723—
SolventDimethylformamideHCID 6228—
Product1-(3-Nitro-4-phenylmethoxyphenyl)ethanoneHCID 11265720—

Reaction Steps

1-(4-hydroxy-3-nitro-phenyl)-ethanone was treated with benzyl bromide in the presence of K2CO3 in DMF, and processed as reported in the synthesis of example 20a to obtain the crude product which was purified using flash chromatography (silica gel, 5% CH3CN in chloroform). Yield, 94%; mp, 132° C.; MS (CI): 300 (M++29), 272 (M++1), 91; analysis: C15H13NO4 requires, C, 66.42; H, 4.83; N, 5.16. found; C, 66.58; H, 4.52; N, 5.30%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964628B2
Source datasetuspto-grants-2011_06
ORD IDord-df808e0f648247e7885d7964c8b9c623
Source noteuspto-grants-2011_06