Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Butanoic acid, 2-bromo-, ethyl ester | HCID 79039 | — |
| Reactant | 4-cyclopropanecarbonylphenol | HCID 1051512 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117701134 | HCID 117701134 | 87.6% |
Reaction Steps
Tripotassium phosphate (8.17 g, 38.5 mmol) and ethyl 2-bromobutyrate (4.77 mL, 32.6 mmol) were added to an acetone (24 mL) solution of cyclopropyl(4-hydroxyphenyl)methanone (4.80 g, 29.6 mmol) at room temperature, and the mixture was stirred for 4 hours under reflux. Tripotassium phosphate (1.57 g, 7.40 mmol) and ethyl 2-bromobutyrate (1.08 mL, 7.40 mmol) were added to the mixture at room temperature, and the resulting mixture was stirred for 3 hours under reflux. After the reaction mixture was cooled to room temperature, water was added to the reaction mixture, and the resulting mixture was extracted once with acetone. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1→1:1, v/v). Subsequently, the compound thus obtained was dissolved in water (45 mL), then 5 M aqueous sodium hydroxide solution (8.78 mL, 44.4 mmol) was added to the mixture at room temperature, and the resulting mixture was stirred at the same temperature for 2 hours. Water and a saturated aqueous solution of ammonium chloride were added to the reaction mixture, and the mixture was extracted three times with ethyl acetate, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. Carbonyldiimidazole (7.20 g, 44.4 mmol) was added to a tetrahydrofuran (150 mL) solution of the compound thus obtained (7.35 g, 29.5 mmol) at room temperature, and the mixture was stirred at the same temperature for 30 minutes. A 28% aqueous ammonia solution (30 mL, excess amount) was added to the mixture at room temperature, and the resulting mixture was stirred at the same temperature for 30 minutes. Water was added to the reaction mixture, and the resulting mixture was extracted three times with ethyl acetate, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1→ethyl acetate, v/v) to give the title compound (6.41 g, yield: 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233958B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-d5d7e659e3634c93ba831a7ca89aebbf |
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| Source note | uspto-grants-2016_01 |
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