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HRID 2858作成日:2026年10月23日

Potassium Iodide → (+/-)-trans-2-Butyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline

https://huagongshe.com/ja/reaction/2858

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Butyl bromideHCID 8002—
反応物Potassium CarbonateHCID 11430—
反応物(+/-)-trans-4a-(3-Methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline hydrochlorideHCID 86752321—
溶媒DimethylformamideHCID 6228—
生成物(+/-)-trans-2-Butyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinolineHCID 8675232324.9%

反応手順

0.71 g (2.55 mmol) of (±)-trans-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline hydrochloride, 0.37 g (2.68 mmol) of butyl bromide, 0.53 g of potassium carbonate and a catalytical amount of potassium iodide in 15 ml of DMF were reacted as described in preparation 20, yielding 0.2 g of the title compound which was used as such in the subsequent step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731322
出典データセットuspto-grants-1998_03
ORD IDord-9cef4a5077a74084b0f66091336f0c5e
出典メモuspto-grants-1998_03