HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648701Generated: October 29, 2026
Acetic Acid → methyl 3-oxo-3,4-dihydro-2H-1,5-benzodioxepin-2-carboxylate
https://huagongshe.com/reaction/648701
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-methoxycarbonylmethyloxyphenoxyacetate | HCID 347859 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | methyl 3-oxo-3,4-dihydro-2H-1,5-benzodioxepin-2-carboxylate | HCID 13544514 | 74.4% |
Reaction Steps
To a mixture of 4.1 g of 60% sodium hydride in 150 ml of xylene is added 0.3 ml of tert-butanol, and a solution of 10 g of methyl 2-methoxycarbonylmethyloxyphenoxyacetate in 100 ml of xylene is added dropwise to the mixture at 140°-150° C. (for 8 hours). To the reaction mixture 7 g of acetic acid is added and the precipitates are filtered off. The filtrate is concentrated under reduced pressure, and the residue is purified by column chromatography on silica gel (eluant: hexane:ethyl acetate=3:1 2:1), to give 6.5 g of methyl 3-oxo-3,4-dihydro-2H-1,5-benzodioxepin-2-carboxylate as a colorless oil. Mass spectrum m/e: 222 (M+). IR νmaxneat cm-1 : 1750. NMR (CDCl3) δ: 3.75(3H, singlet, OCH3), 4.68 (2H, double doublet, C4 --H), 5.32 (1H, singlet, C2 --H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04736031 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-562e2a4bd99b498fa9d59924ef611652 |
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| Source note | uspto-grants-1988_04 |
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