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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclooctylamine | HCID 2903 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-[Bis(4-methoxymethoxyphenyl)methyl]benzaldehyde | HCID 19938143 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(Cyclooctyl)-2-[bis(4-methoxymethoxyphenyl)methyl]benzylamine | HCID 19938097 | 89.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05413997 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-c97e50d097fd4a3aae5ba7b68380f0cf |
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| Source note | uspto-grants-1995_05 |
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