HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107265Generated: October 25, 2026
Tetrahydrofuran → Ethyl 3-(2-anilinothiazol-4-yl)acrylate
https://huagongshe.com/reaction/2107265
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| Reactant | 2-Anilinothiazole-4-carbaldehyde | HCID 15053570 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-(2-anilinothiazol-4-yl)acrylate | HCID 54052926 | — |
Reaction Steps
A mixture comprising 3.5 g of 2-anilinothiazole-4-carbaldehyde, 6.5 g of (ethoxycarbonylmethylene)triphenylphosphorane and 35 ml of tetrahydrofuran was heated at 60 ° C. for 2 hours. The reaction mixture was poured into water and extracted with benzene. The benzene extract was dried over anhydrous sodium sulfate, and the solvent was evaporated off under reduced pressure, giving an oil. This oil was purified by silica gel column chromatography. using as eluent a 9:1 mixture of benzene and ethyl acetate, giving the desired compound as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04933355 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-7f3200267c1946fc93d2bec920aa06e4 |
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| Source note | uspto-grants-1990_06 |
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