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HRID 422142作成日:2026年10月26日

Diglyme → (1S,2R,4aS,8aS)-1-(3,5-dimethoxyphenoxymethyl)-2,5,5,8a-tetramethyl-decahydronaphthalen-2-ol

https://huagongshe.com/reaction/422142

反応式

関与物質

役割名称HCID仕込み量
反応物DiglymeHCID 8150—
反応物Cesium carbonateHCID 10796—
反応物1-Iodo-3,5-dimethoxybenzeneHCID 640179—
反応物(1S,2R,4aS,8aS)-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-decahydronaphthalen-2-olHCID 10879261—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物(1S,2R,4aS,8aS)-1-(3,5-dimethoxyphenoxymethyl)-2,5,5,8a-tetramethyl-decahydronaphthalen-2-olHCID 5829481270.4%

反応条件

温度120 °C

反応手順

In a sealed tube purged with nitrogen, 1-iodo-3,5-dimethoxybenzene (36) (0.78 g, 3.0 mmol), (1S,2R,4aS,8aS)-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-decahydronaphthalen-2-ol (3) (0.65 g, 2.68 mmol), Cs2CO3 (1.3 g, 4.0 mmol), 3,4,7,8-tetramethyl-[1,10]-phenylthroline (0.12 g, 0.50 mmol), CuI (0.05 g, 0.3 mmol), diglyme (2 mL) and toluene (10 mL) were added. The reaction mixture was stirred at 120° C. for 18 h. The reaction was cooled to room temperature, diluted with EtOAc (300 mL) and washed with water (100 mL). The organic layer was dried (Na2SO4) and concentrated. Purification by column chromatography on silica gel (Hexanes/EtOAc, 2:1) gave (1S,2R,4aS,8aS)-1-(3,5-dimethoxyphenoxymethyl)-2,5,5,8a-tetramethyl-decahydronaphthalen-2-ol (37) (0.71 g, 70%) as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101605B2
出典データセットuspto-grants-2012_01
ORD IDord-17c99bf7cc9046eb816ff65e957a6ff5
出典メモuspto-grants-2012_01