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HRID 402778作成日:2026年10月26日

Acetic Anhydride → Ethyl 4-(acetylamino)-3-ethoxybenzoate

https://huagongshe.com/reaction/402778

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Benzoic acid, 4-amino-3-ethoxy-, ethyl esterHCID 825957—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 4-(acetylamino)-3-ethoxybenzoateHCID 6676515570.6%

反応手順

To a 100 mL round bottom flask were added ethyl 4-amino-3-ethoxybenzoate (1.3 g, 6.2 mmol), TEA (2.6 mL, 18.6 mmol), N,N-dimethylpyridin-4-amine (catalytic), acetic anhydride (0.88 mL, 9.3 mmol) and EtOAc (20 mL). The reaction mixture was stirred at ambient temperature for 3 hours and was then diluted with EtOAc (20 mL) and washed with 5% KOH (50 mL). The organic layer was dried over Na2SO4, filtered and concentrated. The crude product was purified on a silica gel column eluting with a gradient of EtOAc/hexanes to give the title intermediate (1.1 g) as a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742110B2
出典データセットuspto-grants-2014_06
ORD IDord-027a69ab6c71446ba26610b17c2ed133
出典メモuspto-grants-2014_06