Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Morpholinoacetophenone | HCID 38362 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Trimethylphosphonoacetate | HCID 53413272 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 66868250 | HCID 66868250 | 69.9% |
Reaction Steps
To a chilled (0° C.) solution of potassium tert-butoxide (1.0 M, 37.1 mL) was dropwise added a solution of trimethylphosphonoacetate, keeping the temperature below 25° C. The solution was then allowed to warm to room temperature and stirred for an additional five minutes, after which a solution of 4-morpholinoacetophenone in THF (20 mL) was added in one portion. The solution was slowly heated to 60° C. for 36 hours. The solution was cooled to room temperature, then diluted with a 1.0N HCl solution (100 mL), and extracted with ethyl acetate (2×100 mL). The organic layers were combined and dried over MgSO4, filtered, and the filtrate concentrated to a white solid which was recrystallized from hexane/ethyl acetate to give 3.33 grams of 3-(4-morpholinophenyl)but-2-enoic acid methyl ester intermediate (69.9% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212155B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-29173d97f6c147938cf46dae0fbbfe42 |
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| Source note | uspto-grants-2015_12 |
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