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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264541생성일: 2026년 10월 26일

Ammonia → 2-(2-Oxoethyl)-5-methoxy-1-tetralone

https://huagongshe.com/reaction/264541

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물PhosphateHCID 1061—
반응물Ammonium ChlorideHCID 25517—
반응물2-(2,2-dimethoxy-1-ethyl)-5-methoxy-1-tetralone N,N-dimethylhydrazoneHCID 67714266—
촉매Cupric chloride dihydrateHCID 61482—
용매TetrahydrofuranHCID 8028—
생성물2-(2-Oxoethyl)-5-methoxy-1-tetraloneHCID 1903637280%

반응 단계

280 mg of 2-(2,2-dimethoxy-1-ethyl)-5-methoxy-1-tetralone N,N-dimethylhydrazone were dissolved in 12.5 ml of THF and added to 5 ml of phosphate buffer (prepared from 2 ml of 1/15M potassium dihydrogen phosphate and 3 ml of 1/15M disodium hydrogen phosphate) as well as 156 mg of copper (II) chloride dihydrate. After stirring at room temperature for 3.5 hours, the reaction had finished. The mixture was treated with 10 ml of 20% ammonium chloride solution and 0.8 ml of conc ammonia. Then, the mixture was extracted several times with ethyl acetate, dried over sodium sulfate, filtered and evaporated. The residue was chromatographed on silica gel firstly with toluene, then with toluene/ethyl acetate 9:1. 180 mg (80%) of 2-(2-oxoethyl)-5-methoxy-1-tetralone were obtained as a yellowish oil (Rf=0.31, silica gel (toluene/ethyl acetate 9:1)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646173
출처 데이터셋uspto-grants-1997_07
ORD IDord-1811e1398c7448c0b99f32f53ed03a7f
출처 메모uspto-grants-1997_07