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Methanethiol → 1-[5-(Methylsulfanyl)-4-nitrothiophen-2-yl]ethan-1-one

HRID 544749
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HRID 544749 반응식
[CH3:1][SH:2].Cl[C:4]1[S:5][C:6]([C:12](=[O:14])[CH3:13])=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10].O>C(O)C>[CH3:1][S:2][C:4]1[S:5][C:6]([C:12](=[O:14])[CH3:13])=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10]
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참가 물질

5

반응물 3

HCID 878MethanethiolHCID 962WaterHCID 5211051-(5-Chloro-4-nitrothiophen-2-yl)ethan-1-one

생성물 1

HCID 202136841-[5-(Methylsulfanyl)-4-nitrothiophen-2-yl]ethan-1-one

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

Liquid methylmercaptan (4 ml) was added to a solution of 0.82 g of Na in 50 ml of absolute ethanol. The resulting solution was added to a solution of 7.2 g of 2-chloro-3-nitro-5-acetylthiophene in 200 ml of absolute ethanol in 15 minutes at 5° C. After stirring at room temperature for 30 minutes, 100 ml of water was added, after which the precipitate was sucked off and washed successively with water and isopropanol. The precipitate was boiled a moment with 300 ml of carbontetrachloride, cooled down, and sucked off. After drying the title compound was obtained in a yield of 6.4 g; m.p. 191°-193° C.

후처리

  1. washwashed successively with water and isopropanol
  2. temperaturecooled down
  3. dry with materialAfter drying the title compound
  4. customwas obtained in a yield of 6.4 g

출처 및 근거

ORD 기록
ord-ecb85c68df1b4eb9a34bd7c29ea0387b
출처 데이터셋
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04451660

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