HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448340Generated: October 30, 2026
Sodium Carbonate → N-{1-[2-(2-furanyl)ethyl]-4-(methoxymethyl)-4-piperidinyl}-N-phenylpropanamide ethanedioate
https://huagongshe.com/reaction/1448340
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Noralfentanil | HCID 162172 | — |
| Reactant | 2-(Furan-2-yl)ethyl 4-methylbenzene-1-sulfonate | HCID 10333146 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | N-{1-[2-(2-furanyl)ethyl]-4-(methoxymethyl)-4-piperidinyl}-N-phenylpropanamide ethanedioate | HCID 86734317 | 39.1% |
Reaction Steps
To a stirred and refluxing mixture of 9.5 parts of sodium carbonate and 240 parts of 4-methyl-2-pentanone are added 8.3 parts of N-[4-(methoxymethyl)-4-piperidinyl]-N-phenylpropanamide and 9.6 parts of [2-(2-furanyl)ethyl] 4-methylbenzenesulfonate (water-separator). The whole is stirred and refluxed for 21 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 residue is converted into the ethanedioate salt in 2-propanol. The salt is filtered off and crystallized from 2-propanol, yielding 5.4 parts (39.1%) of N-{1-[2-(2-furanyl)ethyl]-4-(methoxymethyl)-4-piperidinyl}-N-phenylpropanamide ethanedioate; mp. 178.6° 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-6eb8a015c2184c128656232c987b7fb3 |
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| Source note | uspto-grants-1979_12 |
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