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HRID 49691作成日:2026年10月26日

2,6-Dimethoxyphenol → 1,2,3-Trimethoxybenzene

https://huagongshe.com/reaction/49691

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-DimethoxyphenolHCID 7041—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物1,2,3-TrimethoxybenzeneHCID 12462—

反応条件

温度90 °C

反応手順

To a solution of 2,6-dimethoxyphenol (1.0 g, 6.49 mmol) in DMC (10 mL), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (0.99 g, 6.49 mmol) was added and the resulting solution was heated to reflux (90° C.) for 4.5 hours. The reaction was cooled to ambient temperature and diluted with EtOAc (50 mL) and H2O (40 mL). The organic layer was separated and washed in sequence with H2O (40 mL), 2M HCl (2×40 mL), 2M NaOH (2×40 mL) and H2O. The organic layer was dried over Na2SO4, filtered and concentrated under vacuum to give trimethoxybenzene as a solid. The yield of trimethoxybenzene as determined by HPLC was 99%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706929B2
出典データセットuspto-grants-2004_03
ORD IDord-74f981d105f24b61a718cb4381b6bd64
出典メモuspto-grants-2004_03