HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6971Generated: October 25, 2026
Methyl p-toluenesulfonate → 3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl ester
https://huagongshe.com/reaction/6971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl ester | HCID 2758867 | 56% |
Reaction Steps
To a solution of ethyl 4,4,4-trifluoroacetoacetate (12 mL, 82 mmol) in DMF (80 mL) is added cesium carbonate (26.4 g, 82 mmol). The reaction mixture is heated to 70° C. A solution of methyl p-toluenesulfonate (13.5 mL, 90 mmol) in DMF (30 mL) is then added dropwise during 30 min and the reaction mixture is stirred for an additional 1 hr. After cooling to room temperature, the reaction mixture is diluted with H2O (150 mL) and extracted with Et2O (2×150 mL). The organic extracts are combined and washed with H2O and brine, then dried (Na2SO4), filtered and concentrated to afford the title compound (9.0 g, 56%) as an oil which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084170B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-d146ffc4743f46cfb9a96289a70a2846 |
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| Source note | uspto-grants-2006_08 |
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