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m-Chloroperbenzoic acid → HCID 20232107、化合物

HRID 2290337
ノート
印刷プレビュー

反応式

HRID 2290337 の反応式
ClC1C=CC=C(C(OO)=[O:9])C=1.[CH3:12][C:13]1[N:14]=[C:15]([S:25][CH3:26])[N:16]=[N:17][C:18]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C(Cl)(Cl)Cl>[CH3:12][C:13]1[N:14]=[C:15]([S:25]([CH3:26])=[O:9])[N:16]=[N:17][C:18]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 155863425-Methyl-3-methylthio-6-phenyl-1,2,4-triazine

生成物 1

HCID 20232107HCID 20232107、化合物収率 88.5%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

m-Chloroperbenzoic acid (20 g) was added to a stirred solution of 5-methyl-3-methylthio-6-phenyl-1,2,4-triazine (20 g) in chloroform (600 ml) under ice cooling, and the mixture was stirred for 30 minutes at room temperature. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate, dried over sodium sulfate, and then concentrated. The resulting residue was crystallized with diethyl ether, and the crystals were collected by filtration, washed with diethyl ether and dried to give 5-methyl-3-methylsulfinyl-6-phenyl-1,2,4-triazine (19.0 g).

後処理

  1. washThe reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate
  2. dry with materialdried over sodium sulfate
  3. concentrationconcentrated
  4. customThe resulting residue was crystallized with diethyl ether
  5. filtrationthe crystals were collected by filtration
  6. washwashed with diethyl ether
  7. customdried

出典と根拠

ORDレコード
ord-a4b4184592cf4e1da36ce71f8b34d588
出典データセット
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04616014

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート