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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24366생성일: 2026년 10월 23일

Water → 5-Methoxyoxindole

https://huagongshe.com/ko/reaction/24366

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물5-MethoxyisatinHCID 38333—
용매Ethyl AcetateHCID 8857—
생성물5-MethoxyoxindoleHCID 151428615.2%

반응 단계

A mixture of 5-methoxyisatin (5.0 g) and 30 ml of hydrazine hydrate was refluxed for 15 minutes. The reaction mixture was cooled to room temperature and 50 ml of water was added. The mixture was extracted 3 times with 25 ml of ethyl acetate, the organic layers combined, dried over anhydrous sodium sulfate and concentrated to give a yellow solid. The solid was stirred in ethyl acetate and 1.1 g of insoluble material removed by vacuum filtration and saved. This material proved to be 2-hydrazinocarbonylmethyl-4-anisidine. The filtrate was concentrated and chromatographed on silica gel eluting with ethyl acetate:hexane 1:1 to give 0.7 g of 5-methoxy-2-oxindole as a dirty yellow solid. The 1.1 g of 2-hydrazinocarbonylmethyl-4-anisidine was refluxed for 1 hour in 20 ml of 1 N sodium hydroxide. The mixture was cooled, acidified to pH 2 with concentrated hydrochloric acid and extracted 3 times with 25 ml of ethyl acetate. The organic extracts were combined, washed with brine, dried over anhydrous sodium sulfate and concentrated to give 0.8 g of 5-methoxy-2-oxindole as a dirty yellow solid. The combined yield was 1.5 g or 33%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-ad136b85cbcc4a9080c2cc92707ce764
출처 메모uspto-grants-2005_02