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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 502197생성일: 2026년 10월 26일

Ethanol → 6-Iodoindoline

https://huagongshe.com/reaction/502197

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium HydroxideHCID 14798—
반응물1-Acetyl-6-iodoindolineHCID 11666396—
용매WaterHCID 962—
생성물6-IodoindolineHCID 1161569664%

반응 단계

1-Acetyl-6-iodoindoline (1.06 g, 3.7 mmol), NaOH (1.16 g, 29 mmol), EtOH (8 mL), and H2O (6 mL) are heated at 90° C. overnight. The reaction mixture is then partitioned between H2O and EtOAc. The organic layer is extracted into aqueous HCl. The aqueous layer is in turn basified with NaOH, and is extracted with EtOAc. The organic layer is dried and concentrated. Hexane trituration yields 6-iodoindoline (577 mg, 64%) as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772271B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-cccbf76f7a2c4761a39a138ca4e0cc4d
출처 메모uspto-grants-2010_08