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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219754생성일: 2026년 10월 24일

Iodine → 3-(2-Ethoxyphenyl)-3-hydroxy-5-iodoindol-2-one

https://huagongshe.com/ko/reaction/219754

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Ammonium ChlorideHCID 25517—
반응물2-BromophenetoleHCID 68500—
반응물5-IodoisatinHCID 88695—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-(2-Ethoxyphenyl)-3-hydroxy-5-iodoindol-2-oneHCID 57466442—

반응 조건

온도20 °C

반응 단계

4 g (164 mMol) of magnesium turnings and 5% of the total amount of 2-bromo-1-ethoxybenzene were put into 20 ml of ether and, after addition of a little iodine, were heated until the reaction started. 33.1 g (165 mMol) of 2-bromo-1-ethoxybenzene dissolved in 100 ml of ether were slowly added dropwise to the boiling solution in such a way that the reaction continued with gentle boiling. Then, while cooling slightly to 20° C., 15 g (54.9 mMol) of 5-iodoisatin in 400 ml of anhydrous tetrahydrofuran were added dropwise. The mixture was then stirred at room temperature for 2 h. The reaction solution was poured into an aqueous NH4Cl solution with stirring. This aqueous phase was extracted several times with ethyl acetate, and the combined aqueous phase was washed four times with water, dried and concentrated in vacuo, resulting in the product as a crystalline precipitate. 19.2 g of the product were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202870B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-f588b2f796754e5b9d1ed63240c9f62f
출처 메모uspto-grants-2012_06