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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31353생성일: 2026년 10월 23일

Iodine → 5,6-Dichloro-3-hydroxy-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/ko/reaction/31353

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물2-BromoanisoleHCID 11358—
반응물MagnesiumHCID 5462224—
반응물5,6-dichloro-1H-indole-2,3-dioneHCID 11009341—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물5,6-Dichloro-3-hydroxy-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-oneHCID 2192550274%

반응 단계

5.57 g of 1-bromo-2-methoxybenzene are added dropwise to a suspension of 0.72 g of magnesium in 15 ml of ether containing a few crystals of iodine, the reflux being maintained once it has started. At the end of the addition, the mixture is refluxed for 2 hours. A suspension of 2.7 g of 5,6-dichloro-1H-indole-2,3-dione in 30 ml of THF is then added and the mixture is refluxed for 30 minutes. After cooling to RT, the reaction mixture is poured into a water/ice/-concentrated HCl mixture and extracted with EtOAc, the organic phase is dried over Na2SO4 and the solvent is evaporated off under vacuum. The residue is slurried in hot iso ether and the precipitate formed is spin-filtered off and washed with ether. 3 g of the expected product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425566B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-8a70d1b019c341bfa8531040820b3ea8
출처 메모uspto-grants-2008_09