HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973038Generated: October 30, 2026
2,2-Diethoxyethylamine → HCID 12707053, compound
https://huagongshe.com/reaction/973038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Reactant | 3,5-Dibenzyloxybenzaldehyde | HCID 561351 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12707053 | HCID 12707053 | 100.6% |
Reaction Steps
4.6 g of 3,5-dibenzyloxybenzaldehyde are added to 3.0 g of 1-amino-2,2-diethoxyethane, and the mixture is heated at 100° C for 10 minutes. Then, the mixture is stirred at 60° C for 2.5 hours under reduced pressure until water is removed from the mixture. 6.3 g of 1-[N-(3,5-dibenzyloxybenzylidene)amino]-2,2-diethoxyethane is thereby obtained as an oil. 5.9 g of this product are dissolved in 100 ml of ethanol. 600 mg of sodium borohydride are added to the ethanol solution, and the mixture is refluxed for 2 hours. After the reaction, water is added to the mixture and the aqueous mixture is extracted with ethyl acetate. The extract is dried and then evaporated to remove solvent, whereby 5.9 g of 1-[N-(3,5-dibenzyloxybenzyl)amino]-2,2-diethoxyethane are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04054659 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-7ae8c77a0f604c888d95f02247b0c37a |
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| Source note | uspto-grants-1977_10 |
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