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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 884생성일: 2026년 10월 23일

N-Methyl-N-Methoxy-4-(3-indolyl)butyramide → Benzyl-3-(3-indolyl)propyl ketone

https://huagongshe.com/ko/reaction/884

반응식

참여 물질

역할이름HCID투입량
반응물N-Methyl-N-Methoxy-4-(3-indolyl)butyramideHCID 11107631—
반응물HCID 178418336HCID 178418336—
용매TetrahydrofuranHCID 8028—
생성물Benzyl-3-(3-indolyl)propyl ketoneHCID 5706426468.6%

반응 단계

To a solution of 147 mg (0.60 mmol) of amide 139 in 4.0 mL of THF at -78° C. was added 1.31 mL (1.31 mmol) of benzylmagnesium chloride (1.0M in Et2O) and the reaction mixture was allowed to warm to room temperature and stir for 3 h. The reaction was quenched with 5% KHSO4 and extracted into ether. The combined ethereal layers were washed with brine and dried over MgSO4. Flash chromatography (elution with 25% ether in hexane) gave 108 mg of the ketone 140. 1H NMR consistent with structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723459
출처 데이터셋uspto-grants-1998_03
ORD IDord-70019092bb2c48d18020b5be4b31c9ad
출처 메모uspto-grants-1998_03