HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601898Generated: November 1, 2026
Water → (1-Benzyl-4-phenylpiperidin-4-yl)methanamine
https://huagongshe.com/reaction/1601898
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 reaction mixture is stirred for 1 hour at RT and then heated for 1 hour at 40° C. It is cooled in an ice bath and 3 ml of water, 3 ml of 4 N NaOH solution and 12 ml of water are added successively. The mineral salts are filtered off and the filtrate is evaporated under vacuum. The residue is chromatographed on silica H using a gradient of a DCM/MeOH mixture (from 100/3; v/v to 100/10; v/v) as the eluent to give 11 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977359 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-51d4befe1e4a4621b4b170c3554455f6 |
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| Source note | uspto-grants-1999_11 |
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