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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972833Generated: October 26, 2026

Water → Ethyl 5-(2-methyl-5-thiazolyl)-2,4-pentadienoate

https://huagongshe.com/reaction/972833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthyl diethylphosphonocrotonateHCID 7022350—
Reactant2-Methyl-1,3-thiazole-5-carbaldehydeHCID 13934728—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-(2-methyl-5-thiazolyl)-2,4-pentadienoateHCID 5425269198.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 12.5 g of ethyl diethylphosphonocrotonate in 25 ml of tetrahydrofuran was added with stirring to a mixture of 100 ml of anhydrous tetrahydrofuran and 3 g of sodium hydride in 46% of an oil cooled to 0°C and the mixture was stirred for 30 minutes at 0°C. Then, a mixture of 6.4 g of 2-methyl-5-thiazolecarboxaldehyde in 25 ml of tetrahydrofuran was added to the mixture at 0°C and 250 ml of ice and 250 ml of water were added. The mixture was extracted with methylene chloride and the organic extracts were washed with water, dried and filtered. The filtrate was evaporated to dryness under reduced pressure to obtain 13 g of raw product which was dissolved in ether and the ether solution was stirred in the presence of Florosil and then with activated carbon. The mixture was filtered and the filtrate was evaporated to dryness under reduced pressure to obtain 11 g of ethyl 5-(2-methyl-5-thiazolyl)-2,4-pentadienoate in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04053618
Source datasetuspto-grants-1977_10
ORD IDord-e9e6cf7cf0514329be9064b9f11e32d7
Source noteuspto-grants-1977_10