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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410712Generated: November 3, 2026

Diethyl Ether → 3-Ethoxycarbonyl-2-methoxycarbonyl-but-2-enoic acid methyl ester

https://huagongshe.com/reaction/1410712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDimethyl malonateHCID 7943—
ReactantEthyl pyruvateHCID 12041—
CatalystZincchlorideHCID 3007855—
SolventAcetic AnhydrideHCID 7918—
Product3-Ethoxycarbonyl-2-methoxycarbonyl-but-2-enoic acid methyl esterHCID 8671410968.9%

Reaction Steps

A mixture of ZnCl2 (53 g, 388 mmol) in acetic anhydride (120 mL) was stirred at r.t. for 2 h. The resulting solution was decanted, and to this solution was added ethyl pyruvate (25 g, 215 mmol) and dimethyl malonate (25 mL, 215 mmol). The resulting mixture was heated at 100° C. for 1 h, then left standing at r.t. for 16 h. Ether (300 mL) was added and the mixture was washed with ice water (5×300 mL) and saturated NaHCO3 (2×300 mL). The organic layer was dried over MgSO4 and concentrated to give a dark brown oil, which was distilled under reduced pressure to give 34.1 g of the title compound as an orange oil. 1H NMR (CDCl3, 200 MHz): δ=4.26 (q, 2H, J=7.0 Hz), 3.82 (s, 3H), 3.79 (s, 3H), 2.22 (s, 3H), 1.32 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921389B2
Source datasetuspto-grants-2014_12
ORD IDord-daaf00d81e70439b93d6ae2956a19d7e
Source noteuspto-grants-2014_12