HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580049Generated: October 29, 2026
Ethanol → 6,11-Dihydro-11-oxodibenz[b,e]oxepin-2-propanoic acid
https://huagongshe.com/reaction/580049
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | 4-(2-Carboxybenzyloxy)phenylpropanoic acid | HCID 12292313 | — |
| Product | 6,11-Dihydro-11-oxodibenz[b,e]oxepin-2-propanoic acid | HCID 12392960 | 68% |
Reaction Steps
Phosphorus pentoxide (10.4 g, 0.073 mole) was cautiously added to 7.4 ml of absolute ethanol under a nitrogen atmosphere and stirred at 110° C. for 1 hour; 53.1 ml of sulfolane was added and the temperature adjusted to 85° C. After adding 4-(2-carboxybenzyloxy)phenylpropanoic acid of Example 6a (5.0 g, 0.017 mole), the reaction was stirred at 85° C. for 3.5 hours. The mixture was poured into 1 liter of ice water, made basic by addition of NaOH pellets, extracted with toluene and the aqueous phase was then acidified with concentrated HCl. The resulting precipitate was filtered, triturated with isopropanol and dried giving 3.22 g of 6,11-dihydro-11-oxodibenz[b,e]oxepin-2-propanoic acid (68% yield), m.p. 128°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04751238 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-c958176abf6940f79bdeea82b0cd0d6d |
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| Source note | uspto-grants-1988_06 |
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