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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230019Erstellt: 25. Oktober 2026

4-tert-Butylcyclohexylamine → HCID 178468863, Verbindung

https://huagongshe.com/reaction/230019

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-tert-ButylcyclohexylamineHCID 79396—
EduktEthyl 4-acetylbenzoateHCID 600911—
EduktSodium borohydrideHCID 4311764—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelEthanolHCID 702—
ProduktHCID 178468863HCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07563815B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-ab23a8b3691249bdbcf244877fbb3fd8
Quellennotizuspto-grants-2009_07