HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236777Generated: October 26, 2026
2-Bromopropane → 4-(Methoxymethyl)-N-phenyl-1-(propan-2-yl)piperidin-4-amine
https://huagongshe.com/reaction/236777
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | N,N-Diethylacetamide | HCID 12703 | — |
| Reactant | 4-(Methoxymethyl)-N-phenylpiperidin-4-amine | HCID 18319932 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-(Methoxymethyl)-N-phenyl-1-(propan-2-yl)piperidin-4-amine | HCID 23339040 | 42.6% |
Reaction Steps
A mixture of 10 parts of 2-bromopropane, 9 parts of 4-(methoxymethyl)-N-phenyl-4-piperidinamine, 4.9 parts of N,N-diethylethanamide and 72 parts of N,N-dimethylacetamide is stirred and refluxed for 10.25 hours. After cooling, the formed N,N-diethylethanamine hydrobromide is filtered off and the filtrate is diluted with water. The product is extracted with methylbenzene. The extract is washed thoroughly with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 5.7 parts (42.6%) of 4-(methoxymethyl)-1-(1-methylethyl)-N-phenyl-4-piperidinamine as an oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04157393 |
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| Source dataset | uspto-grants-1979_06 |
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| ORD ID | ord-3cb8a07bc3fd4993b51c0996b0c2daab |
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| Source note | uspto-grants-1979_06 |
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