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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252571생성일: 2026년 10월 25일

Ethanol → 6-Iodoindoline

https://huagongshe.com/reaction/252571

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 번호US07868037B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-a0f13259a14d43c5b16fbd2049ae4af8
출처 메모uspto-grants-2011_01