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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660703Generated: October 26, 2026

Butyrophenone → 2-(3-Benzyloxy-4-nitrobenzyl)-1-phenylbutan-1-one

https://huagongshe.com/reaction/660703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyrophenoneHCID 10315—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Benzyloxy-4-bromomethyl-1-nitrobenzeneHCID 62115042—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Benzyloxy-4-nitrobenzyl)-1-phenylbutan-1-oneHCID 68837950—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-phenylbutan-1-one (203 mg, 1.37 mmol) in THF (2.5 mL) at −78° C. is added dropwise LiHMDS (1.62 mL of 1.0 M solution in THF, 1.62 mmol) over a period of 15 min. The solution is stirred at −78° C. for 1 h then a solution of 2-benzyloxy-4-bromomethyl-1-nitrobenzene (Example 83, step C) (400 mg, 1.25 mmol) in THF (2.5 mL) is added dropwise. The mixture is allowed to warm to RT and stirred there for 1 h then is quenched with saturated ammonium chloride solution. The mixture is extracted with EtOAc and the organic phase is washed with brine then dried over magnesium sulfate. The solvent is removed under reduced pressure and the residue is purified by flash chromatography using a gradient of 5-100% EtOAc/hexane as eluent to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-8d07e62cd094468fb85af82de7512bca
Source noteuspto-grants-2011_12