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HRID 457550생성일: 2026년 10월 24일

2-Methyl-2-butene → 4-Iodo-2-methoxypyridine-3-carboxylic acid

https://huagongshe.com/ko/reaction/457550

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-buteneHCID 10553—
반응물4-Iodo-2-methoxynicotinaldehydeHCID 10038381—
반응물Sodium ChloriteHCID 23668197—
반응물Monosodium phosphateHCID 23672064—
용매Formic AcidHCID 284—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
용매TetrahydrofuranHCID 8028—
생성물4-Iodo-2-methoxypyridine-3-carboxylic acidHCID 1843994067%

반응 단계

To a solution of 4-iodo-2-methoxy-pyridine-3-carbaldehyde (4.96 g, 18.9 mmol) in 22 mL tert.-butanol was added in this order 2-methyl-2-butene (30 mL of a 2 M solution in THF, 60 mmol), natriumdihydrogen-phosphate (5.7 g, 47.5 mmol), water (15 mL) and sodiumchlorite (3.9 g, 43 mmol). The mixture was stirred at ambient temperature for 1 hour, then poured on dilute aqueous formic acid. The mixture was extracted with ethyl acetate, the organic layer washed with water and brine and concentrated. The residue was dissolved in diisopropylether+dichloromethane (1+1) and extracted 3 times with half-concentrated aqueous NaOH solution. The combined aqueous layers were acidified with conc. HCl and extracted with ethyl acetate. The organic layers were washed with water and brine, then dried over sodium sulfate and concentrated to give 3.462 g of the title compound as a white solid (67%). 1H NMR (500 MHz, CD3OD) δ 7.83 (d, J=5.4 Hz, 1H), 7.43 (d, J=5.4 Hz, 1H), 3.94 (s, 3H);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07189716B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-95f44250f2ae4abf80b18a4681f20a35
출처 메모uspto-grants-2007_03