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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36441Generated: October 27, 2026

Cyclooctylamine → N-(Cyclooctyl)-2-[bis(4-methoxymethoxyphenyl)methyl]benzylamine

https://huagongshe.com/reaction/36441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclooctylamineHCID 2903—
ReactantSodium borohydrideHCID 4311764—
Reactant2-[Bis(4-methoxymethoxyphenyl)methyl]benzaldehydeHCID 19938143—
SolventEthanolHCID 702—
ProductN-(Cyclooctyl)-2-[bis(4-methoxymethoxyphenyl)methyl]benzylamineHCID 1993809789.4%

Reaction Steps

In 50 ml of ethanol was dissolved 0.69 g of cyclooctylamine. To the solution was added 1.96 g of 2-[bis(4-methoxymethoxyphenyl)methyl]benzaldehyde obtained by Reference Example 3, and the mixture was stirred overnight. Then, 0.85 g of sodium borohydride was added thereto, and the reaction mixture was stirred for 2 hours. Thereafter, the solvent was evaporated under reduced pressure, and water was added to the residue. The aqueous mixture was extracted with chloroform, and the organic layer was separated. The aqueous layer was extracted with chloroform, and the organic layer was combined and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography to afford 2.25 g of the desired product (Compound 77) as an oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05413997
Source datasetuspto-grants-1995_05
ORD IDord-c97e50d097fd4a3aae5ba7b68380f0cf
Source noteuspto-grants-1995_05