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HRID 22167作成日:2026年10月24日

Hydrochloric Acid → 3-Acetoxy-7-[(4,6-dimethoxy-pyrimidin-2-yl)oxy]-phthalide

https://huagongshe.com/ja/reaction/22167

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Acetyl chlorideHCID 6367—
反応物TriethylamineHCID 8471—
反応物7-[(4,6-Dimethoxy-pyrimidin-2-yl)oxy]-3-hydroxy-phthalideHCID 19927417—
溶媒TetrahydrofuranHCID 8028—
生成物3-Acetoxy-7-[(4,6-dimethoxy-pyrimidin-2-yl)oxy]-phthalideHCID 19927387—

反応手順

1.3 g of 7-[(4,6-dimethoxy-pyrimidin-2-yl)oxy]-3-hydroxy-phthalide (see Example 84) are dissolved in 10 ml of tetrahydrofuran, and 0.6 ml of triethylamine is added to the solution which is then treated dropwise at 25° C. (internal temperature) with 0.5 ml of acetyl chloride. After subsequently stirring for 2 hours at room temperature, the reaction mixture is treated with ice-water and dilute hydrochloric acid and extracted with ethyl acetate, and the organic phase is washed with sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. Column chromatography on silica gel [eluant: ethyl acetate/n-hexane (2:3)] yields 3-acetoxy-7-[(4,6-dimethoxy-pyrimidin-2-yl)oxy]-phthalide in the form of white crystals, m.p. 119°-120° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428002
出典データセットuspto-grants-1995_06
ORD IDord-6e8bbe39c65b4649a8217bfb868323d0
出典メモuspto-grants-1995_06