HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 855238Erstellt: 24. Oktober 2026
Water → N'-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamine
https://huagongshe.com/de/reaction/855238
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| Edukt | 1,2-Ethanediamine, N1-ethyl-N1-(3-methylphenyl)- | HCID 87984 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N'-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamine | HCID 69342865 | 95% |
Reaktionsschritte
1.62 g (10 mmol) of 4-tert-butyl benzaldehyde and 1.78 g (10 mmol) of N*1*-ethyl-N*1* -m-tolyl-ethane-1,2-diamine were dissolved in 20 ml methanol and the solution was stirred for 2 h at rt. 567 mg (15 mmol) of sodium borohydride were added in portions under nitrogen. The reaction mixture was stirred at rt over night. Water was added and the solvent was evaporated. The reaction mixture was extracted with diethyl ether and the organic layer was washed with saturated aqueous NaCl solution, dried over sodium sulfate, filtered and the solvent was evaporated to leave the 3.08 g (95%) product as a light yellow oil. 1H NMR (DMSO-d6, 300 MHz): δ 7.33 (d, 2H), 7.24 (d, 2H), 7.09 (dd, 1H), 6.51 (m, 3H), 3.78 (s, 2H), 3.42 (t, 2H), 3.34 (q, 2H), 2.85 (t, 2H), 2.29 (s, 3H), 1.31 (s, 9H), 1.11 (t, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07259183B2 |
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| Quelldatensatz | uspto-grants-2007_08 |
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| ORD ID | ord-f8163ec0f6c446e3a9d9efb6fbe68099 |
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| Quellennotiz | uspto-grants-2007_08 |
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