HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283535Generated: October 31, 2026
Water → N-Ethyl-1-(1-piperidinyl)cyclohexanemethanamine
https://huagongshe.com/reaction/1283535
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 21409872 | HCID 21409872 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Ethyl-1-(1-piperidinyl)cyclohexanemethanamine | HCID 21409821 | 67.6% |
Reaction Steps
A solution of 1-[1-(acetamidomethyl)cyclohexyl] piperidine (5.5 g.) in dry tetrahydrofuran (50 ml) was added dropwise with stirring during 10 mins. to a suspension of lithium aluminium hydride (3.8 g.) in dry tetrahydrofuran (100 ml). The mixture was heated under reflux for 51/2 hrs. and stirred at room temperature for 16 hrs. Water (10 ml) was added dropwise to decompose excess lithium aluminium hydride (grey suspension had turned white). The suspension was filtered through hyflo, washed with ether and the combined filtrates dried (anhyd. Na2SO4). The dried filtrate was evaporated to dryness under reduced pressure and the residual oil (5 g.) was distilled under high vacuum to give 1-[1-(Ethylaminomethyl)cyclohexyl]piperidine (3.5 g.). b.p. C 138°-144° at 5.5 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03975443 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-f6cc3bf129f144f9b14d24358f3f93e9 |
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| Source note | uspto-grants-1976_08 |
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