HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236173Generated: October 31, 2026
Chlorosuccinimide → Ethyl 5-chloro-2-phenyloxazole-4-carboxylate
https://huagongshe.com/reaction/2236173
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Ethyl 2-phenyl-1,3-oxazole-4-carboxylate | HCID 571056 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 5-chloro-2-phenyloxazole-4-carboxylate | HCID 67537623 | 37.7% |
Reaction Steps
Mixture of 2-phenyl-oxazole-4-carboxylic acid ethyl ester (217 mg, 1 mmol), 1-chloro-pyrrolidine-2,5-dione (400 mg, 3 mmol) and two drops of sulfuric acid in chloroform (10 mL) was heated at 90 degrees for overnight. After the reaction was complete, solvent was evaporated. To the residue, water was added, and then the mixture was extracted with ethyl acetate twice. The organic layers were collected, combined, washed with saturated sodium bicarbonate, dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck silica gel 60, 230-400 mesh, 5-40% ethyl acetate in hexane for 30 min) gave 5-chloro-2-phenyl-oxazole-4-carboxylic acid ethyl ester (95 mg, 37%) as a white solid. LCMS calcd for C12H10ClNO3 (m/e) 251, obsd 252 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714126B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-c38f396e6def4bf5836fc95da9ebe164 |
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| Source note | uspto-grants-2010_05 |
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