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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7143생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/7143

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrogen PeroxideHCID 784—
반응물2,3-LutidineHCID 11420—
용매Acetic AnhydrideHCID 7918—
생성물2-Acetoxymethyl-3-methyl-pyridineHCID 10749557—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084155B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b0ed2b81d0864736adc41f19e2b2dd94
출처 메모uspto-grants-2006_08