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HRID 1682813作成日:2026年10月24日

Toluene → (+)-(4aR)-(10bR)-4-methyl-8-(9-anthracenyl)-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one

https://huagongshe.com/ja/reaction/1682813

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Sodium CarbonateHCID 10340—
反応物(4aR)-(10bR)-4,10b-dimethyl-8-bromo-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-oneHCID 15355317—
反応物9-Anthraceneboronic AcidHCID 15510213—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒ChloroformHCID 6212—
生成物(+)-(4aR)-(10bR)-4-methyl-8-(9-anthracenyl)-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-oneHCID 5401422943%

反応手順

A 15mL round bottom flask was charged with (+)-(4aR)-(10bR)-4-methyl-8-bromo-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one (200 mg, 0.65 mmol), tetrakis(triphenylphosphine) palladium (0) (23 mg, 0.02 mmol), 9-anthracenylboronic acid (159 mg, 0.78 mmol), 0.65 mL of sodium carbonate and 2 mL of toluene, fitted with a reflux condenser, and the stirred mixture was heated at 80°, under nitrogen, for 48 h. The mixture was cooled, diluted with chloroform (75 mL) and washed with brine (2×25 mL). The combined organic extracts were dried over sodium sulfate, concentrated, and purified by silica gel chromatography (EtOAc eluent) to give 112 mg (43%) of the title compound as an amorphous solid. mp 95°-110°. FDMS: m/e=405. α[D]589 45.73 (c=0.66, chloroform).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05635197
出典データセットuspto-grants-1997_06
ORD IDord-0949f4cde7404eaa8973eac658e4c246
出典メモuspto-grants-1997_06