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HRID 218351作成日:2026年10月26日

Methanol → Methyl 5-[(2E)-3-(dimethylamino)prop-2-enoyl]-2-methoxybenzoate

https://huagongshe.com/reaction/218351

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物Methyl 5-acetyl-2-methoxybenzoateHCID 606426—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 5-[(2E)-3-(dimethylamino)prop-2-enoyl]-2-methoxybenzoateHCID 5801547790.1%

反応条件

温度95 °C

反応手順

Methyl 5-acetyl-2-methoxybenzoate (11.98 g, 48.0 mmol) was added to N,N-dimethylformamide dimethyl acetal (44.6 g, 374.5 mmol) held under a nitrogen atmosphere. The resulting solution was heated at 95° C. for 60 minutes. Methanol (10 ml) was then removed by atmospheric distillation and further N,N-dimethylformamide dimethyl acetal (8.90 g, 74.9 mmol) added. The resulting solution was heated at 95° C. for a further 270 minutes. The reaction was then cooled to 50° C. and ethyl acetate (35 mL) added. Solvent (35 mL) is removed from the reaction by atmospheric distillation and fresh ethyl acetate (35 mL) added. Further solvent (35 mL) is removed from the reaction by atmospheric distillation and fresh ethyl acetate (50 mL) added. The reaction mixture is cooled to RT whereby the desired product crystallises out as a granular, free flowing solid. The solid was isolated by filtration, washed twice with fresh ethyl acetate (2×30 mL) and dried to constant weight to afford 11.39 g of the desired methyl 5-[(2E)-3-(dimethylamino)prop-2-enoyl]-2-methoxybenzoate (8).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198441B2
出典データセットuspto-grants-2012_06
ORD IDord-8e86a24c94064261b40e8b03092a0b64
出典メモuspto-grants-2012_06