HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1511595Erstellt: 25. Oktober 2026
Sodium borohydride → 2,2-diethoxy-N-(thiophen-2-ylmethyl)ethanamine
https://huagongshe.com/reaction/1511595
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 2,2-Diethoxy-N-(thiophen-2-ylmethylene)ethaneamine | HCID 21821170 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2,2-diethoxy-N-(thiophen-2-ylmethyl)ethanamine | HCID 2795396 | 71,9% |
Reaktionsschritte
2,2-Diethoxy-N-(thiophen-2-ylmethylene)ethaneamine (100 g) prepared in the step 1 was dissolved in 500 mL of dry ethanol, then 18.3 g of sodium borohydride was slowly added thereto little by little at room temperature and the mixture was stirred overnight at room temperature. The solvent was evaporated from the reaction solution in vacuo and the residue was poured over 300 mL of a 10% aqueous solution of acetic acid. The resulting aqueous solution was washed with diethyl ether, neutralized with 10% aqueous ammonia and subjected to extraction with diethyl ether. The organic layer was washed with water and a saturated solution of sodium chloride successively and dried over anhydrous magnesium sulfate and the solvent was evaporated therefrom in vacuo to give 72.5 g of the objective compound as colorless liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08217031B2 |
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| Quelldatensatz | uspto-grants-2012_07 |
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| ORD ID | ord-d5921d32063e4ba0b245f82bc0d86b5c |
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| Quellennotiz | uspto-grants-2012_07 |
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