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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 562913생성일: 2026년 10월 24일

Isopropyl iodide → Methyl 2-(3-cyano-4-isopropoxyphenyl)isonicotinate

https://huagongshe.com/ko/reaction/562913

반응식

참여 물질

역할이름HCID투입량
반응물Isopropyl iodideHCID 6362—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 2-(3-cyano-4-hydroxyphenyl)isonicotinateHCID 136368377—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Methyl 2-(3-cyano-4-isopropoxyphenyl)isonicotinateHCID 6699504195.2%

반응 단계

In 5 ml of DMF were dissolved 82 mg of methyl 2-(3-cyano-4-hydroxyphenyl)isonicotinate and 66 mg of isopropyl iodide, and the resulting solution was heated at 80° C. for 3 hours in the presence of 72 mg of potassium carbonate and 10 mg of tetra-n-butylammonium bromide. The reaction solution was cooled and then diluted with water, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried and concentrated under reduced pressure. The resulting residue was washed with a mixed solvent (hexane:ethyl acetate=10:1) to obtain 91 mg of methyl 2-(3-cyano-4-isopropoxyphenyl)isonicotinate. (2) Then, 86 mg of the compound was dissolved in a mixed solution of 3 ml of methanol and 3 ml of THF, and 0.35 ml of a 1M aqueous sodium hydroxide solution was added thereto, followed by heating at 60° C. for 1 hour. After being cooled to room temperature, the resulting solution was diluted with diisopropyl ether and water and an aqueous layer was separated. The aqueous layer was neutralized with 1M hydrochloric acid and then extracted with ethyl acetate. After being washed with water, the organic layer was dried and concentrated under reduced pressure to obtain 55 mg of 2-(3-cyano-4-isopropoxyphenyl)isonicotinic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067446B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-f3e080e16a49494697220dc0092501c6
출처 메모uspto-grants-2011_11