HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597263Generated: October 31, 2026
Water → (1-Benzyl-4-phenylpiperidin-4-yl)methanamine
https://huagongshe.com/reaction/1597263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Benzyl-4-cyano-4-phenylpiperidine | HCID 191408 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Benzyl-4-phenylpiperidin-4-yl)methanamine | HCID 804238 | 54.2% |
Reaction Steps
A suspension of 2.8 g of lithium aluminum hydride in 50 ml of THF is cooled to 0° C. and a solution of 20 g of 1-benzyl-4-cyano-4-phenylpiperidine in 50 ml of THF is added dropwise. The mixture is kept stirring for 1 hour at RT and then heated at 40° C. for 1 hour. The reaction mixture is cooled on an ice bath, and 3 ml of water, 3 ml of a 4N solution of NaOH and 12 ml of water are added successively. The inorganic salts are filtered and the filtrate evaporated under vacuum. The residue is chromatographed on silica H, eluting with the gradient of the DCM/MeOH mixture from (100/3; v/v) to (100/10; v/v). 11 g of the expected product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06294537B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-178d0cad4cc04375a2a0ab5afd5a7f55 |
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| Source note | uspto-grants-2001_09 |
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