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Water → 2-(3-Iodophenyl)-5-methyl-1,3,4-thiadiazole

HRID 1672791
ノート
印刷プレビュー

反応式

HRID 1672791 の反応式
C1(C)C=CC=CC=1.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:17])=CC=1.[C:30]([NH:33][NH:34][C:35](=O)[C:36]1[CH:41]=[CH:40][CH:39]=[C:38]([I:42])[CH:37]=1)(=O)[CH3:31].O>C(OCC)(=O)C>[I:42][C:38]1[CH:37]=[C:36]([C:35]2[S:17][C:30]([CH3:31])=[N:33][N:34]=2)[CH:41]=[CH:40][CH:39]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 1140TolueneHCID 87949Lawesson's reagentHCID 824395HCID 824395、化合物

生成物 1

HCID 193499822-(3-Iodophenyl)-5-methyl-1,3,4-thiadiazole収率 60.4%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
120 °C

実験手順

Toluene (4.1 mL) and Lawesson's reagent (366 mg, 0.904 mmol) were added to N′-acetyl-3-iodobenzohydrazide (250 mg, 0.822 mmol) obtained in Step 1, and the mixture was stirred at 120° C. for 1 hour. After cooling, water and ethyl acetate were added to the mixture to separate the organic layer. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was then purified by silica gel column chromatography to give 2-(3-iodophenyl)-5-methyl-1,3,4-thiadiazole (150 mg, 60%).

後処理

  1. temperatureAfter cooling
  2. customto separate the organic layer
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure
  5. customThe resulting residue was then purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-57390878c68a49b288a5e393d50076c3
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07998954B2

反応ノート

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