돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1243317생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1243317

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 2192550280.6%

반응 단계

7.5 g of 1-bromo-2-methoxybenzene are added dropwise to a suspension of 1.1 g of magnesium in 20 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 heated at reflux for 2 hours. A suspension of 4.3 g of 5,6-dichloro-1H-indole-2,3-dione in 20 ml of THF is then added and the resulting 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 triturated in hot iso ether and the precipitate formed is filtered off by suction and washed with ether. 5.2 g of the expected product are obtained, m.p.=245–246° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07119086B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-565d91cc6fda462198d18bd8a8f68e27
출처 메모uspto-grants-2006_10