HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286685Generated: November 1, 2026
Sodium borohydride → HCID 12875598, compound
https://huagongshe.com/reaction/2286685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 12875557 | HCID 12875557 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12875598 | HCID 12875598 | — |
Reaction Steps
A mixture of 5.55 parts of 1-(diphenylmethyl)-N-[(6-methyl-2-pyridyl)methylene]-4-piperidinamine, 1.9 part of sodium borohydride and 250 parts by volume of ethanol is stirred at room temperature for about two hours. The reaction mixture is evaporated to dryness in vacuo, the residue partitioned between 200 parts by volume of water and 150 parts by volume of methylene chloride and the layers separated. The aqueous layer is extracted with additional 125 parts by volume of methylene chloride. The methylene chloride fractions are combined, washed with 200 parts by volume of water, dried over anhydrous sodium sulfate, filtered and evaporated to dryness in vacuo to yield, as a yellow oil, 1-(diphenylmethyl)-N-[(6-methyl-2-pyridyl)methyl]-4-piperidinamine. This compound has the following formula ##STR35##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04267318 |
|---|
| Source dataset | uspto-grants-1981_05 |
|---|
| ORD ID | ord-5d693a17e53742498b5bf27b1fe2b642 |
|---|
| Source note | uspto-grants-1981_05 |
|---|