HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660561Generated: October 31, 2026
Sulfuryl chloride → Ethyl 3-(2-chloro-4-fluorophenyl)-3-oxopropanoate
https://huagongshe.com/reaction/1660561
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Ethyl 3-(4-Fluorophenyl)-3-Oxopropanoate | HCID 2758844 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 3-(2-chloro-4-fluorophenyl)-3-oxopropanoate | HCID 54191286 | 88.3% |
Reaction Steps
A mixture of 10.5 g (0.05 mole) of ethyl p-fluorobenzoylacetate, 6.7 g (0.05 mole) of sulfuryl chloride and 30 ml. of chloroform was held at reflux for 18 hours and cooled. The chloroform solution was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was distilled to give 10.8 g (88%) of ethyl 2-chloro-(p-fluoro)-benzoylacetate as an oil. A mixture of 10.8 g (0.441 mole) of ethyl 2-chloro-(p-fluoro)-benzoylacetate, 3.36 g (0.0441 mole) of thiourea, 20 ml. of water and 10 ml. of ethanol was held at reflux for 3 hours. Ethanol was removed under reduced pressure. The residue was made basic with saturated sodium bicarbonate. The solid was filtered, washed with water and recrystallized from ethanol to give 8.9 g (76%) of ethyl 2-amino-4-(p-fluorophenyl)-5-thiazolecarboxylate as white prisms, m.p. 205°-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04308391 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-9f3494f8aebb43b9be54d9ff970ec623 |
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| Source note | uspto-grants-1981_12 |
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