HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658354Generated: October 30, 2026
Hydrochloric Acid → HCID 68491667, compound
https://huagongshe.com/reaction/658354
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Ethoxy-1,1,1-trifluoro-3-buten-2-one | HCID 2780395 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68491667 | HCID 68491667 | 67.3% |
Reaction Steps
Diethyl malonate (33.7 g, 0.2 mol) was dissolved in acetonitrile (200 mL), and magnesium chloride (21.4 g, 0.22 mol) was slowly added thereto at 0 to 5° C. After 10 minutes, triethylamine (44.5 g, 0.44 mol) was added dropwise thereto at 0 to 5° C., and the mixture was allowed to react for 1 hour at room temperature. To the reaction mixture, 4-ethoxy-1,1,1-trifluoro-3-butene-2-one (37.0 g, 0.22 mol) was added dropwise at 0 to 5° C., and the mixture was allowed to react for 1 hour at room temperature. The reaction mixture was poured into diluted hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water, dried, and concentrated. Thus obtained oily product was dissolved in toluene (100 mL), p-toluenesulfonic acid (5 g) was added thereto, and the mixture was allowed to react for 3 hours under heating. After cooling, the solvent was distilled off, and thus obtained crystal was recrystallized from ethyl acetate, to obtain 31.8 g of a desired product (yield: 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076487B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-8a1a2f2acec948b08fd7ff72056f33f1 |
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| Source note | uspto-grants-2011_12 |
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