4-tert-Butylcyclohexylamine → HCID 178445668, compound

Participants

Reaction Steps

A mixture of 5-bromo-1-indanone (6.33 g, 30.0 mmol), titanium (IV) isopropoxide (17.8 mL, 60.0 mmol), 4-tert-butylcyclohexyl amine (9.32 g, 60.0 mmol) in absolute ethanol (200 mL) was stirred under nitrogen at room temperature for 8 h. Sodium borohydride (1.70 g, 45.0 mmol) was then added and the resulting mixture was stirred for an additional 18 h at room temperature. The reaction was quenched by pouring into aqueous ammonia (2N, 300 mL). The resulting inorganic precipitate was filtered off through Celite and washed with CH2Cl2 (300 mL). The organic layer was separated and the remaining aqueous layer was extracted once with CH2Cl2 (100 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated. Chromatography (10% to 20% EtOAc in Hexane) afforded (5-bromo-2,3-dihydro-1H-inden-1-yl)(trans-4-tert-butylcyclohexyl). HPLC/MS: m/z=350.1, (M+1), Rt=3.01 min. 1H NMR (CDCl3): δ 7.38 (1H, br s), 7.34 (1H, d, J=8.0 Hz), 7.24 (1H, d, J=8.0 Hz), 4.32 (1H, t, J=6.5 Hz), 3.00 (1H, ddd, J=5.0 Hz, 8.0 Hz, 16.0 Hz), 2.81 (1H, dt, J=8.0 Hz, 16.0 Hz), 2.61 (1H, m), 2.46 (1H, m), 2.08 (1H, m), 2.00 (1H, m), 1.86-1.78 (4H, m), 1.20-1.04 (4H, m), 0.90 (9H, s).

Provenance & Evidence