HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980872Generated: October 30, 2026
Methyl iodide → 1-Benzyl-3-methyl-4-piperidone
https://huagongshe.com/reaction/980872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzyl-3-methyl-4-piperidone | HCID 560965 | 39.4% |
Reaction Steps
At first, 4.2 g of 60% sodium hydride was suspended in 200 ml of tetrahydrofuran, and then a solution of 18.9 g of 1-benzyl-4-piperidone and 17.9 g of methyl iodide dissolved in 20 ml of tetrahydrofuran was added dropwise to the suspension at room temperature over 5 minutes. Thereafter, the mixture was heated to 60° C. and stirred for 5 hours. Thereafter, the reaction mixture was filtered. The filtrate was concentrated, and then the concentrate was poured into 150 ml of water and extracted with 120 ml portions of ethyl acetate three times. The extract was washed with 150 ml of brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 21.6 g of an oily matter. The oily matter was purified by silica gel column chromatography (eluent: n-hexane:ethyl acetate=2:1 V/V) to obtain 8.0 g of 1-benzyl-3-methyl-4-piperidone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04639522 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-e6ee90eb5bee4a0b9be8c8a2ce183781 |
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| Source note | uspto-grants-1987_01 |
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