HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28125Generated: October 29, 2026
Sodium borohydride → N-[1-(phenylmethyl)-4-piperidinyl]-3-pyridinamine
https://huagongshe.com/reaction/28125
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[1-(phenylmethyl)-4-piperidinylidene]-3-pyridinamine | HCID 10706822 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[1-(phenylmethyl)-4-piperidinyl]-3-pyridinamine | HCID 10706957 | — |
Reaction Steps
To a stirred solution of 27 parts of N-[1-(phenylmethyl)-4-piperidinylidene]-3-pyridinamine in 40 parts of ethanol are added portionwise 3.8 parts of sodium borohydride. After the addition is complete, the whole is heated to 50° C. The solvent is evaporated. The oily residue is dissolved in 150 parts of hydrochloric acid IN and filtered. The filtrate is rendered alkaline with ammonium hydroxide and extracted with methylbenzene. The organic layer is dried over magnesium sulfate, filtered and evaporated. The solid residue is washed with 2,2'-oxybispropane and dried, yielding 14 parts of N-[1-(phenylmethyl)-4-piperidinyl]-3-pyridinamine; mp. 131°-133° C.; beige, amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04225606 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-6ec1545350424b409648c95f9caadd8d |
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| Source note | uspto-grants-1980_09 |
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