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HRID 7143作成日:2026年10月25日

Acetic Acid → 2-Acetoxymethyl-3-methyl-pyridine

https://huagongshe.com/reaction/7143

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrogen PeroxideHCID 784—
反応物2,3-LutidineHCID 11420—
溶媒Acetic AnhydrideHCID 7918—
生成物2-Acetoxymethyl-3-methyl-pyridineHCID 10749557—

反応手順

To a stirred solution of 2,3-lutidine (4.8363 g, 45.13 mmol) in glacial acetic acid (30 mL) at room temperature was added 30% H2O2 (4.6 mL) and the resultant solution was heated to 70° C. After 6 hours, the reaction mixture was cooled to room temperature, additional H2O2 (4.6 mL) was added, and the solution was heated at 70° C. overnight. The reaction mixture was allowed to cool to room temperature and then concentrated under reduced pressure. The residue was dissolved in CHCl3 (100 mL) and treated with solid Na2CO3 (14.12 g). After 1 hour, the supernatant was decanted and the residue was washed with warm CHCl3 (3×50 mL). The combined supernatants were filtered and concentrated to provide 4.6951 g as a yellow solid. The solid was dissolved in acetic anhydride (38 mL) and heated at 90° C. overnight. The mixture was cooled to room temperature and concentrated and the crude product was filtered through a silica plug (33 g silica, ethyl acetate) to give 6.13 g of 2-acetoxymethyl-3-methyl-pyridine as an orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084155B2
出典データセットuspto-grants-2006_08
ORD IDord-b0ed2b81d0864736adc41f19e2b2dd94
出典メモuspto-grants-2006_08