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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3374생성일: 2026년 10월 23일

Tetrahydrofuran → N-Methoxy-N-methylcyclopropanecarboxamide

https://huagongshe.com/ko/reaction/3374

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물N-tert-butoxycarbonyl-3-methoxy-2-methylanilineHCID 10609918—
반응물[2-(Tert-butoxycarbonylamino)-6-methoxyphenyl]methyl cyclopropyl ketoneHCID 10804518—
반응물CID 53628100HCID 178418400—
용매CyclohexaneHCID 8078—
생성물N-Methoxy-N-methylcyclopropanecarboxamideHCID 15643267—

반응 단계

Using the procedure described in Example 9, Part A, 100 mL (130 mmol) of 1.3M sec-butyl lithium in cyclohexane was reacted with N-tert-butoxycarbonyl-3-methoxy-2-methylaniline (15.4 g, 65 mmol) in 100 mL of THF and then with 8.4 g (65 mmol) of N-methoxy-N-methylcyclopropylcarboxamide to give crude [2-(tert-butoxycarbonylamino)-6-methoxyphenyl]methyl cyclopropyl ketone. This material on treatment with 20 mL of trifluoroacetic acid in 300 mL of methylene chloride for 6 hours gave a material that was chromatographed on silica gel. Eluting with a gradient, toluene→5% EtOAc/toluene, there was obtained 6.4 g (52% yield) of 2-cyclopropyl-4-methoxy-1H-indole as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733923
출처 데이터셋uspto-grants-1998_03
ORD IDord-34fde6f5003d4e6dab0c33bf86ba9d7f
출처 메모uspto-grants-1998_03