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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161404Generated: October 27, 2026

N-Formylmorpholine → 8-methoxy-4H-benzo[1,3]dioxine-6-carbaldehyde

https://huagongshe.com/reaction/1161404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FormylmorpholineHCID 20417—
ReactantAmmonium ChlorideHCID 25517—
Reactant6-bromo-8-methoxy-4H-benzo[1,3]dioxineHCID 59511816—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product8-methoxy-4H-benzo[1,3]dioxine-6-carbaldehydeHCID 13266818—

Reaction Conditions

Temperature-72 °C

Reaction Steps

To a solution of 31.2 g of 6-bromo-8-methoxy-4H-benzo[1,3]dioxine in 500 ml of THF there was added dropwise 55 ml of n-butyllithium (2.55 M, hexane solution) at −70° C. under a nitrogen atmosphere. After stirring at −72° C. for 30 minutes, 20 ml of N-formylmorpholine was added and the temperature was raised from −78° 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 (21.28 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816522B2
Source datasetuspto-grants-2010_10
ORD IDord-80975df076eb4ee3b41592664c49cde5
Source noteuspto-grants-2010_10