HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230019Erstellt: 25. Oktober 2026
4-tert-Butylcyclohexylamine → HCID 178468863, Verbindung
https://huagongshe.com/reaction/230019
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-tert-Butylcyclohexylamine | HCID 79396 | — |
| Edukt | Ethyl 4-acetylbenzoate | HCID 600911 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Katalysator | Titanium isopropoxide | HCID 11026 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 178468863 | HCID 178468863 | — |
Reaktionsschritte
A mixture of ethyl 4-acetylbenzoate (3.00 g, 15.6 mmol), titanium (IV) isopropoxide (9.30 mL, 31.2 mmol), 4-tert-butylcyclohexyl amine (4.85 g, 31.2 mmol) in absolute ethanol (100 mL) was stirred under nitrogen at room temperature for 10 h. Sodium borohydride (0.88 g, 23.4 mmol) was then added and the resulting mixture was stirred for an additional 8 h at room temperature. The reaction was quenched by pouring into aqueous ammonia (2N, 225 mL). The resulting inorganic precipitate was filtered off and washed with dichloromethane (100 mL). The organic layer was separated and the remaining aqueous layer was extracted once with dichloromethane (100 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated. Chromatography (20% EtOAc in Hexane) afforded ethyl 4-{1-[(trans-4-tert-butylcyclohexyl)amino]ethyl}benzoate. HPLC/MS: m/z=332.3 (M+1), Rt=2.74 min. 1HNMR (500 MHz, CDCl3): δ 8.01 (2H, d, J=8.1 Hz), 7.38 (2H, d, J=8.0 Hz), 4.37 (2H, q, J=7.1 Hz), 4.02 (1H, q, J=6.6 Hz), 2.18-2.06 (2H, m), 1.77-1.67 (4H, m), 1.39 (3H, t, J=7.1 Hz), 1.32 (3H, d, J=6.5 Hz), 1.22 (1H, br s), 1.09-0.85 (4H, m), 0.79 (9H, s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07563815B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-ab23a8b3691249bdbcf244877fbb3fd8 |
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| Quellennotiz | uspto-grants-2009_07 |
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