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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1416010생성일: 2026년 10월 26일

Ammonium Chloride → 2-benzyloxy-N-[1-(3,5-dichlorophenylthio)-3-methyl-2-oxobutyl]-N-methylacetamide

https://huagongshe.com/reaction/1416010

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물3,5-DichlorophenylsulfideHCID 21187117—
반응물2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)acetamideHCID 22130912—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2-benzyloxy-N-[1-(3,5-dichlorophenylthio)-3-methyl-2-oxobutyl]-N-methylacetamideHCID 2213068647%

반응 조건

온도-78 °C

반응 단계

In 2 ml of dry tetrahydrofuran was dissolved 100 mg (0.4 mmol )of 2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)acetamide (18a'), and there was added 223 μl (0.4 mmol)of n-butyllithium (1.7 M hexane solution)with stirring at -78° C. over 10 minutes. After stirring at -78° C. for 1 hour, and a tetrahydrofuran solution (1 ml)of 135 mg (0.4 mmol)of 3,5-dichlorophenylsulfide was added thereto over 10 minutes. After 30 minutes, the temperature was raised up to room temperature, a saturated aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate ester. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was purified by silica gel chromatography (hexane/ethyl acetate 5:1)to give 79 mg of 2-benzyloxy-N-[1-(3,5-dichlorophenylthio)-3-methyl-2-oxobutyl]-N-methylacetamide (20)(yield 47%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05910506
출처 데이터셋uspto-grants-1999_06
ORD IDord-eff25180eddf4bb88481975cbe0a97d5
출처 메모uspto-grants-1999_06