HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161441Generated: October 29, 2026
Hydrochloric Acid → 5-Fluoro-8-methoxychroman-6-carboaldehyde
https://huagongshe.com/reaction/1161441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pentamethyldiethylenetriamine | HCID 18196 | — |
| Reactant | N-Formylmorpholine | HCID 20417 | — |
| Reactant | 5-Fluoro-8-methoxychromane | HCID 59511814 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Fluoro-8-methoxychroman-6-carboaldehyde | HCID 59511862 | — |
Reaction Steps
To a solution of 3.6 g of 5-fluoro-8-methoxychromane and 4.2 ml of N,N,N′,N′,N″-pentamethyldiethylenetriamine in 130 ml of THF there was added dropwise 8 ml of n-butyllithium (2.55 M, hexane solution) at −74° C. After stirring at −74° C. for 1 hour, N-formylmorpholine was added. After further stirring at room temperature for 1 hour, 1N hydrochloric acid was added to the reaction mixture while cooling on ice, and the mixture was extracted with ethyl acetate and 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 (1.50 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816522B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-6d60e4385aca4e568c147f45ddc70db9 |
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| Source note | uspto-grants-2010_10 |
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