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

HRID 544749
ノート
印刷プレビュー

反応式

HRID 544749 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-ecb85c68df1b4eb9a34bd7c29ea0387b
出典データセット
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04451660

反応ノート

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