HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23684Erstellt: 25. Oktober 2026
N,N,N',N'-Tetramethylethylenediamine → Tert-butyl 2-{4-[(dimethylamino)methyl]phenyl}-2-hydroxyethyl(methyl)carbamate
https://huagongshe.com/reaction/23684
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 4-Dimethylaminomethylbenzaldehyde | HCID 193251 | — |
| Edukt | tert-butyl N,N-dimethylcarbamate | HCID 312724 | — |
| Edukt | CID 53628100 | HCID 178418400 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Tert-butyl 2-{4-[(dimethylamino)methyl]phenyl}-2-hydroxyethyl(methyl)carbamate | HCID 22574342 | 76,3% |
Reaktionsschritte
To a solution of tert-butyl dimethylcarbamate (350 mg, 2.4 mmol) and tetramethylethylenediamine (511 mg, 4.4 mmol) in THF (anhydrous, 10 mL) was added sec-butyllithium (1.4 M in cyclohexane, 2.2 mL, 3.1 mmol) at −78° C. The mixture was stirred at that temperature for 1 hour before 4-[(dimethylamino)methyl]benzaldehyde (J.Heterocycl.Chem.; 26; 1989; 1325-1330)(280 mg, 1.7 mmol) was introduced. The reaction mixture was stirred for 2 hours, warmed to room temperature and stirred for 1 hour. Saturated ammonium chloride aqueous solution (10 mL) was added to quench the reaction after the reaction mixture was cooled to −78° C. The organic phase was separated and the aqueous phase was extracted with dichloromethane. The organic phases were combined, washed with brine and dried over sodium sulfate and concentrated. The residue was purified with a silica gel column to give the title compound (0.40 g) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06852731B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-6511676a45de4e4a8f11cbf1be38cd8d |
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| Quellennotiz | uspto-grants-2005_02 |
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