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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl diethylphosphonocrotonate | HCID 7022350 | — |
| Reactant | 2-Methyl-1,3-thiazole-5-carbaldehyde | HCID 13934728 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 5-(2-methyl-5-thiazolyl)-2,4-pentadienoate | HCID 54252691 | 98.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04053618 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-e9e6cf7cf0514329be9064b9f11e32d7 |
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| Source note | uspto-grants-1977_10 |
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