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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286685Generated: November 1, 2026

Sodium borohydride → HCID 12875598, compound

https://huagongshe.com/reaction/2286685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12875557HCID 12875557—
SolventEthanolHCID 702—
ProductHCID 12875598HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04267318
Source datasetuspto-grants-1981_05
ORD IDord-5d693a17e53742498b5bf27b1fe2b642
Source noteuspto-grants-1981_05