Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Methoxybenzyl chloride | HCID 69994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21593249 | HCID 21593249 | 108.9% |
Reaction Steps
In 6 ml of N,N-dimethylformamide was suspended 0.8 g of 60% sodium hydride and thereto was added dropwise a solution of 1.98 g of 2-piperidone in 8 ml of N,N-dimethylformamide under a stream of argon and with ice cooling. Then, to the mixture was added dropwise a solution of 2.82 g of 3-methoxybenzyl chloride in 8 ml of N,N-dimethylformamide at room temperature. The mixture was stirred at 65° C. for 8 hours. After cooling, to the reaction mixture were added ice-cold water and the mixture was extracted with diethyl ether. The extract was purified by a silica gel column chromatography (chloroform:methanol=20:1) to give 4.3 g of 1-(3-methoxybenzyl)-2-piperidone. This compound was heated in 10 ml of 47% hydrobromic acid for 12 hours. The mixture was made alkaline with addition of sodium carbonate and extracted with chloroform. After removing the solvent at a reduced pressure, 2.3 g (yield 57%) of 1-(3-hydroxybenzyl)-2-piperidone was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401739 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-af6ff230b5144918b6bccb9d0d248745 |
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| Source note | uspto-grants-1995_03 |
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