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HRID 230019作成日:2026年10月27日

4-tert-Butylcyclohexylamine → HCID 178468863、化合物

https://huagongshe.com/reaction/230019

反応式

関与物質

役割名称HCID仕込み量
反応物4-tert-ButylcyclohexylamineHCID 79396—
反応物Ethyl 4-acetylbenzoateHCID 600911—
反応物Sodium borohydrideHCID 4311764—
触媒Titanium isopropoxideHCID 11026—
溶媒EthanolHCID 702—
生成物HCID 178468863HCID 178468863—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07563815B2
出典データセットuspto-grants-2009_07
ORD IDord-ab23a8b3691249bdbcf244877fbb3fd8
出典メモuspto-grants-2009_07