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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 907179생성일: 2026년 10월 26일

Ethanol → 6-Iodoindoline

https://huagongshe.com/reaction/907179

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) were heated at 90° C. overnight. The reaction mixture was then partitioned between H2O and EtOAc. The organic layer was extracted into aqueous HCl. The aqueous layer was in turn basified with NaOH, and was extracted with EtOAc. The organic layer was dried and concentrated. Hexane trituration yielded 6-iodoindoline (577 mg, 64%) as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08013006B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-0ec4d54cb95b4cc78d773166451d5bb4
출처 메모uspto-grants-2011_09