HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446559Generated: October 26, 2026
Potassium Carbonate → tert-Butyl 4-[4-(3-methoxy-3-oxopropyl)piperidin-1-yl]benzoate
https://huagongshe.com/reaction/446559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl 4-fluorobenzoate | HCID 2736444 | — |
| Reactant | Methyl 3-(piperidin-4-yl)propanoate | HCID 10261546 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl 4-[4-(3-methoxy-3-oxopropyl)piperidin-1-yl]benzoate | HCID 86663456 | 32.7% |
Reaction Steps
Methyl 3-(piperidin-4-yl)propanoate (WO2004/92124 A2) (206 mg, 1.11 mmol) was dissolved in N,N-dimethylformamide (10 mL), tert-butyl 4-fluorobenzoate (141 mg, 1.11 mmol) and potassium carbonate (100 mg, 1.11 mmol) were added, and the mixture was stirred at 120° C. under a nitrogen atmosphere for 16 hours. After the reaction was completed, a saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture under ice cooling, and ethyl acetate was further added to separate the layers. The resulting organic layer was separated, washed with saturated sodium chloride solution, and then dried with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by NH silica gel column chromatography (hexane:ethyl acetate, 10:1, v/v) to give the title compound (126 mg; yield, 31%) as a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476253B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-42346772ca714dc69f0744d71a88a445 |
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| Source note | uspto-grants-2013_07 |
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