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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487701Generated: October 30, 2026

Diethyl Malonate → 4-Tert-butyl-2-[5-(2,2-diethoxycarbonylethyl)benzofuran-2-yl]thiazole

https://huagongshe.com/reaction/487701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19603727HCID 19603727—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product4-Tert-butyl-2-[5-(2,2-diethoxycarbonylethyl)benzofuran-2-yl]thiazoleHCID 19092697118%

Reaction Steps

A solution of methylmagnesium bromide in tetrahydrofuran (1N, 15 ml) was added to diethyl malonate (7.33 g) at 0° C. for 10 minutes. The mixture was stirred for 2 hours at ambient temperature. To the mixture, 4-tert-butyl-2-(5-chloromethylbenzofuran-2-yl)thiazole (3.50 g) was added and stirred for 23 hours at 45° C. The resulting mixture was concentrated under reduced pressure and added to the solution of 4N hydrogen chloride in ethyl acetate. The resulting precipitates were collected by filtration and washed with n-hexane and diisopropyl ether to give the salt. The salt was added to the aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate and concentrated under reduced pressure to give 4-tert-butyl-2-[5-(2,2-diethoxycarbonylethyl)benzofuran-2-yl]thiazole (5.80 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296495
Source datasetuspto-grants-1994_03
ORD IDord-86ec82fcde99464caebd515e437cd654
Source noteuspto-grants-1994_03