Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclooctylamine | HCID 2903 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 19938091 | HCID 19938091 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19938123 | HCID 19938123 | 65.5% |
Reaction Steps
In 50 ml of ethanol was dissolved 3 g of cyclooctylamine. To the solution was added 11.41 g of 2-[bis-(4-benzyloxyphenyl)methyl]benzaldehyde obtained by Reference Example 8, and the mixture was heated under reflux for 2 hours. Thereafter, 1.78 g of sodium borohydride was added thereto, and the mixture was heated under reflux for 2 hours. The solvent was evaporated-under reduced pressure, and water was added to the residue. The aqueous mixture was extracted with ether, and the organic layer was separated. The aqueous layer was extracted with ether, and then the organic layers were combined and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was recrystallized to afford 9.19 g of the desired product (Compound 82).
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-52c449ca1bc84ea98aa4feae94779a02 |
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| Source note | uspto-grants-1995_05 |
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