HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374659Generated: October 30, 2026
Hydrochloric Acid → 8-Fluoro-2-formyl-5-methoxytetralone
https://huagongshe.com/reaction/374659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-Fluoro-3,4-dihydro-5-methoxy-1(2H)-naphthalenone | HCID 10856353 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Fluoro-2-formyl-5-methoxytetralone | HCID 18996961 | 113.1% |
Reaction Steps
Sodium hydride (12.7 g) (50% dispersion, washed with hexane) was suspended in dry THF under nitrogen. Ethyl formate (27 g) was added and the mixture was stirred for 20 minutes in an ice/water bath. 5-Methoxy-8-fluoro-1-tetralone (J. Med. Chem. (1973) 1003) (17 g) dissolved in THF was added and the mixture was allowed to warm to room temperature. The mixture was stirred under nitrogen for 24 hours. Methanol was added followed by water. The mixture was poured into water, acidified with conc. HCl (aq) and extracted into CHCl3. The organic phase was dried (MgSO4), filtered and concentrated to give a dark oil (22 g) which solidified on standing. This material was recrystallised from ethyl acetate/hexane to give the above compound, m.p. 66°-68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05480873 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-48af8b61367041eda8da53877cf5afc3 |
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| Source note | uspto-grants-1996_01 |
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