Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl propiolate | HCID 12182 | — |
| Reactant | HCID 14087130 | HCID 14087130 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | HCID 68327941 | HCID 68327941 | 32% |
Reaction Steps
To a stirred solution of 5-(4-fluorophenyl)-1,3,4-oxathiazol-2-one (42.80 g, 217.1 mmol) in o-dichlorobenzene (600 mL) was added ethyl propiolate (66.0 mL, 651 mmol). The mixture was heated overnight at 135° C. and concentrated. The residual oil was purified by flash chromatography using a hexane/ethyl acetate gradient to afford ethyl 3-(4-fluorophenyl)isothiazole-5-carboxylate as a pale golden solid (17.35 g, 32%). The more polar, ethyl 3-(4-fluorophenyl)isothiazole-4-carboxylate isomer (generated in 57/43 ratio versus the desired product) was discarded.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126993B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-6bc323108b634a6f9d3f676f63d19e6a |
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| Source note | uspto-grants-2015_09 |
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