HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Diethoxyethylamine → HCID 12707055, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Reactant | 3,5-Dibenzyloxybenzaldehyde | HCID 561351 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 12707053 | HCID 12707053 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12707055 | HCID 12707055 | — |
Reaction Steps
1-[N-(3,5-dibenzyloxybenzyl)-N-p-tosyl-amino]-2,2-diethoxyethane (VI) is readily obtainable. For example, said compound (VI) is prepared by condensing 3,5-dibenzyloxybenzaldehyde with 1-amino-2,2-diethoxyethane at 60° to 100° C, reducing the resultant 1-[N-(3,5-dibenzyloxybenzylidene)amino]-2,2-diethoxyethane with sodium borohydride in ethanol under refluxing to give 1-[N-(3,5-dibenzyloxybenzyl)amino]-2,2-diethoxyethane, and then reacting said product with p-tosyl chloride in pyridine under ice-cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04054659 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-2645dfb9c7de40aab5ae85c7981d3f68 |
| Source note | uspto-grants-1977_10 |