HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698652Generated: October 26, 2026
N-Formylmorpholine → 8-methoxy-4H-benzo[1,3]dioxine-6-carbaldehyde
https://huagongshe.com/reaction/1698652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Formylmorpholine | HCID 20417 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-bromo-8-methoxy-4H-benzo[1,3]dioxine | HCID 59511816 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 8-methoxy-4H-benzo[1,3]dioxine-6-carbaldehyde | HCID 13266818 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163787B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-e4057f27ab9344e09f503b84ad446bef |
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| Source note | uspto-grants-2012_04 |
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