HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983666Generated: October 31, 2026
Hydrochloric Acid → Ethyl 7-(4-ethoxyphenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate
https://huagongshe.com/reaction/983666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-[(4'-Ethoxy-3-formyl-1,1'-biphenyl-4-yl)oxy]butyric acid ethylester | HCID 12070455 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Carbonate | HCID 7766 | — |
| Product | Ethyl 7-(4-ethoxyphenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate | HCID 10759448 | 82% |
Reaction Steps
To a solution of 4-[(4′-ethoxy-3-formyl-1,1′-biphenyl-4-yl)oxy]butyric acid ethylester (0.50 g) in diethyl carbonate (5 ml) was added a solution of 20% sodium ethoxide in ethanol (0.57 g) at room temperature, and the mixture was then heated to 50° C. and stirred for 1 hour. The solution was neutralized with 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed, and concentrated. The concentrate was purified by silica gel chromatography (n-hexane/ethyl acetate=10/1) and subsequent concentration of the appropriate eluate gave white crystal of the title compound (0.39 g, yield 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06864367B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-3e7829c67aaa421d907d420286db94a7 |
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| Source note | uspto-grants-2005_03 |
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