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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-ButanolHCID 6386—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-methoxycarbonylmethyloxyphenoxyacetateHCID 347859—
SolventO-XyleneHCID 7237—
Productmethyl 3-oxo-3,4-dihydro-2H-1,5-benzodioxepin-2-carboxylateHCID 1354451474.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736031
Source datasetuspto-grants-1988_04
ORD IDord-562e2a4bd99b498fa9d59924ef611652
Source noteuspto-grants-1988_04