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3-Chlorobenzoic Acid → 5-Benzenesulfinyl-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole

HRID 1198368
ノート
印刷プレビュー

反応式

HRID 1198368 の反応式
[C:1]1([S:7][C:8]2[CH:31]=[CH:30][C:11]3=[N:12][N:13]([C:15]4[CH:20]=[C:19]([C:21]([CH3:24])([CH3:23])[CH3:22])[CH:18]=[C:17]([C:25]([CH3:28])([CH3:27])[CH3:26])[C:16]=4[OH:29])[N:14]=[C:10]3[CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.ClC1C=C(C=CC=1)C(OO)=[O:37].ClC1C=C(C=CC=1)C(O)=O>C(Cl)Cl>[C:1]1([S:7]([C:8]2[CH:31]=[CH:30][C:11]3=[N:12][N:13]([C:15]4[CH:20]=[C:19]([C:21]([CH3:24])([CH3:22])[CH3:23])[CH:18]=[C:17]([C:25]([CH3:28])([CH3:27])[CH3:26])[C:16]=4[OH:29])[N:14]=[C:10]3[CH:9]=2)=[O:37])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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 4473-Chlorobenzoic AcidHCID 70297m-Chloroperbenzoic acidHCID 193491505-Phenylthio-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole

生成物 1

HCID 193491565-Benzenesulfinyl-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole収率 87.6%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 10.8 g (0.025 mole) of 5-phenylthio-2-(2-hydroxy-3,5-di-tert-butyl-phenyl)-2H-benzotriazole, prepared in Example 2, in 80 mL of methylene chloride is cooled to 3°-5° C. Over a period of 30 min. is added a solution of 5.1 g (0.025 mole) of m-chloroperoxybenzoic acid (MCPBA) 85% in 80 mL of methylene chloride at 3°-5° C. The reaction is stirred for 2 hours at 0°-5° C. with precipitation of m-chlorobenzoic acid. The starting material is shown to be absent. Upon removal of the solvent the residue is dissolved in 200 mL of toluene, m-chlorobenzoic acid is removed by filtration and subsequent washing with 10% aqueous sodium carbonate solution and water. The toluene solution is dried over anhydrous magnesium sulfate, filtered and the solvent removed. The resulting amorphous residue is dissolved in 60 mL of petroleum ether and crystallized. Filtration and washing of the crystals with cold petroleum ether affords 9.8 g (87.6% yield) of the title compound as a solid melting at 152°-154° C.

後処理

  1. temperatureis cooled to 3°-5° C
  2. customUpon removal of the solvent the residue
  3. dissolutionis dissolved in 200 mL of toluene
  4. customm-chlorobenzoic acid is removed by filtration
  5. washsubsequent washing with 10% aqueous sodium carbonate solution and water
  6. dry with materialThe toluene solution is dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customthe solvent removed
  9. dissolutionThe resulting amorphous residue is dissolved in 60 mL of petroleum ether
  10. customcrystallized
  11. filtrationFiltration
  12. washwashing of the crystals with cold petroleum ether

出典と根拠

ORDレコード
ord-051106cc214746e6a207e27f439f3883
出典データセット
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05280124

反応ノート

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