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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698735Generated: October 31, 2026

N-Formylmorpholine → HCID 59517315, compound

https://huagongshe.com/reaction/1698735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FormylmorpholineHCID 20417—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 59517450HCID 59517450—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59517315HCID 59517315—

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 1.3 g of 5-bromo-1,2-dimethoxy-3-(2-methoxy-ethyl)benzene in 20 ml of THF there was added dropwise 2 ml of n-butyllithium (2.66 M, hexane solution) at −70° C. under a nitrogen atmosphere. After stirring at −70° C. for 30 minutes, 0.7 ml of N-formylmorpholine was added and the temperature was raised from −70° C. to 0° C. over a period of 30 minutes. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (806 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163787B2
Source datasetuspto-grants-2012_04
ORD IDord-30a31e6dcfca4f4d9d691e878a8ea0fa
Source noteuspto-grants-2012_04