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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264540생성일: 2026년 10월 26일

2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- → 2-(2,2-dimethoxy-1-ethyl)-5-methoxy-1-tetralone N,N-dimethylhydrazone

https://huagongshe.com/reaction/264540

반응식

참여 물질

역할이름HCID투입량
반응물2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
반응물2-Bromo-1,1-dimethoxyethaneHCID 81672—
반응물5-methoxy-1-tetralone N,N-dimethylhydrazoneHCID 290941—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2-(2,2-dimethoxy-1-ethyl)-5-methoxy-1-tetralone N,N-dimethylhydrazoneHCID 6771426637%

반응 단계

3.12 g of 5-methoxy-1-tetralone N,N-dimethylhydrazone and 4.15 ml of DMPU were dissolved in 70 ml of absolute THF under argon and cooled to -75°. 10.7 ml of a 1.6M solution of n-butyllithium in hexane were added dropwise. The mixture was stirred at -75° for 1 hour and thereupon treated slowly with 2.0 ml of bromoacetaldehyde dimethyl acetal. The mixture was left to warm to room temperature and stirred for 26 hours. 20 ml of water were added at about 0° and the mixture was extracted three times with ethyl acetate. After drying over sodium sulfate, the mixture was filtered, evaporated and the residue was chromatographed on silica gel with toluene, then with toluene/ethyl acetate 9:1. 1.62 g (37%) of 2-(2,2-dimethoxy-1-ethyl)-5-methoxy-1-tetralone N,N-dimethylhydrazone were obtained as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646173
출처 데이터셋uspto-grants-1997_07
ORD IDord-f0ae9af437a8485ebac27d545625552a
출처 메모uspto-grants-1997_07