HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586876Generated: November 2, 2026
Acetic Acid → methyl 1-formyl-7-[4-(2-propoxy)ethoxyphenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylate
https://huagongshe.com/reaction/586876
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Formic anhydride | HCID 9548680 | — |
| Reactant | HCID 22329022 | HCID 22329022 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 1-formyl-7-[4-(2-propoxy)ethoxyphenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylate | HCID 22329024 | — |
Reaction Steps
To anhydrous acetic acid (0.51 ml) was added formic acid, (0.25 ml) at 0° C., and the mixture was stirred at 55° C. for 2 hours, air-cooled and diluted with THF (10 ml). In THF (15 ml) was dissolved methyl 7-[4-(2-propoxy)ethoxyphenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylate (462 mg), and the solution was added dropwise to the previously prepared solution of formic anhydride in THF, at 0° C. The mixture was stirred at room temperature for 2 hours, and the solvent was evaporated under reduced pressure. The residue was diluted with ethyl acetate, washed with saturated sodium hydrogen carbonate solution, water and saturated brine, and dried with anhydrous, magnesium sulfate. The solvent was evaporated under reduced pressure to give crystals, which were washed with ethyl acetate/hexane to give methyl 1-formyl-7-[4-(2-propoxy)ethoxyphenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylate (496 mg) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936602B1 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-875aba5f0f4d484a881b5198b746e910 |
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| Source note | uspto-grants-2005_08 |
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