HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448341Generated: November 1, 2026
Methyl Isobutyl Ketone → HCID 20382323, compound
https://huagongshe.com/reaction/1448341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Noralfentanil | HCID 162172 | — |
| Reactant | 2-(naphthalen-1-yl)ethyl 4-methylbenzenesulfonate | HCID 270483 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20382323 | HCID 20382323 | 43.4% |
Reaction Steps
A mixture of 6.4 parts of sodium carbonate and 120 parts of 4-methyl-2-pentanone is stirred and refluxed with water-separator. Then there are added 4.1 parts of N-[4-(methoxymethyl)-4-piperidinyl]-N-phenylpropanamide and 5.5 parts of [2-(1-naphthalenyl)ethyl]4-methylbenzenesulfonate and the whole is stirred and refluxed for 20 hours. The reaction mixture is cooled to room temperature and poured onto water. The organic phase is separated, washed with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 7% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The oily residue solidifies on triturating in hexane. The product is filtered off and crystallized from a small amount of 2,2'-oxybispropane, yielding 2.8 parts (43.4%) of N-{4-(methoxymethyl)-1-[2-(1-naphthalenyl)ethyl]-4-piperidinyl}-N-phenylpropanamide; mp. 109.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04179569 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-1c924832d49442db8b73fac8b716cc4c |
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| Source note | uspto-grants-1979_12 |
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