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2-Aminothiophenol → HCID 22629953、化合物

HRID 2306872
ノート
印刷プレビュー

反応式

HRID 2306872 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[SH:8].[Cl:9][C:10]1[CH:19]=[C:18]([CH2:20]Cl)[C:13]2[O:14][CH2:15][O:16][CH2:17][C:12]=2[CH:11]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C.C(OCC)(=O)C>[ClH:9].[Cl:9][C:10]1[CH:19]=[C:18]([CH2:20][S:8][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[NH2:1])[C:13]2[O:14][CH2:15][O:16][CH2:17][C:12]=2[CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 87132-AminothiophenolHCID 11430Potassium CarbonateHCID 27767806-Chloro-8-(chloromethyl)-2,4-dihydro-1,3-benzodioxine

生成物 1

HCID 22629953HCID 22629953、化合物

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 8857Ethyl Acetate溶媒

実験手順

2-aminothiophenol (1.25 g, 10 mmol), 6-chloro-8-(chloromethyl)-4H-1,3-benzodioxine (2.17 g, 10 mmol) and potassium carbonate (4.10 g, 30 mmol) were combined in absolute ethanol (100 mL) and stirred 18 h. Dilute with ethyl acetate and wash with saturated sodium bicarbonate solution then brine. The solution was dried over sodium sulfate and the solvent removed in vacuo. The residue was dissolved in methanol and treated with MP BH4− resin (Argonaut 3.16 mmol/g) and potassium carbonate for 48 h. The mixture was filtered and the solvent removed in vacuo. The resulting oil was dissolved in dichloromethane and passed through a 5 g plug of silica gel. The solvent was removed in vacuo and the residue was precipitated from diethyl ether with a solution of hydrogen chloride in dioxane to give the product as an off white powder, 2.52 g (74%). MS (ESI+) for C15H14ClNO2S m/z 308 (M+H)+.

後処理

  1. washwash with saturated sodium bicarbonate solution
  2. dry with materialThe solution was dried over sodium sulfate
  3. customthe solvent removed in vacuo
  4. dissolutionThe residue was dissolved in methanol
  5. additiontreated with MP BH4− resin (Argonaut 3.16 mmol/g) and potassium carbonate for 48 h
  6. filtrationThe mixture was filtered
  7. customthe solvent removed in vacuo
  8. dissolutionThe resulting oil was dissolved in dichloromethane
  9. customThe solvent was removed in vacuo
  10. customthe residue was precipitated from diethyl ether with a solution of hydrogen chloride in dioxane
  11. customto give the product as an off white powder, 2.52 g (74%)

出典と根拠

ORDレコード
ord-56dfbcb2a8f545b8b8125273e12863b8
出典データセット
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06828446B2

反応ノート

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