HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395634Generated: October 29, 2026
Phosphorus oxychloride → Ethyl 2-chloro-4-(5-chloro-2-thienyl)-5-oxazolebutanoate
https://huagongshe.com/reaction/395634
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Ethyl 4-[4-(5-chloro-2-thienyl)-2-oxo-4-oxazolin-5-yl]butanoate | HCID 18174756 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl 2-chloro-4-(5-chloro-2-thienyl)-5-oxazolebutanoate | HCID 12085649 | — |
Reaction Steps
A mixture of ethyl 4-[4-(5-chloro-2-thienyl)-2-oxo-4-oxazolin-5-yl]butanoate (12.5 g), phosphorus oxychloride (24.5 g) and pyridine (3.16 g) was heated to 120-130° C. and stirred for 45 minutes. There action mixture was poured into ice-water (200 ml) and extracted with ethyl acetate (150 ml×2). The organic layer was washed in sequence with a 10% aqueous solution of sodium hydrogen carbonate (100 ml) and a saturated aqueous solution of sodium chloride (100 ml) and dried over anhydrous magnesium sulfate. The organic layer was concentrated, the residue was subjected to silica gel column chromatography, and ethyl 2-chloro-4-(5-chloro-2-thienyl)-5-oxazolebutanoate was obtained as a yellow oil (5.79 g, 48%) from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06605629B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-d77228ccc2bd4641b6a77b789917b137 |
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| Source note | uspto-grants-2003_08 |
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