Sodium Hydroxide → HCID 57939018、化合物

HRID 419933ノート

反応式

HRID 419933 の反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[CH:8][N:7]([CH2:10][CH2:11][OH:12])[C:6]=2[C:13]=1[F:14].P([O-])([O-])([O-])=[O:16].[Na+].[Na+].[Na+].CC1(C)N([O])C(C)(C)CCC1.[O-]Cl=O.[Na+].[O-]Cl.[Na+].[O-]S([O-])=O.[Na+].[Na+].[OH-].[Na+]>O.CC#N>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[CH:8][N:7]([CH2:10][C:11]([OH:16])=[O:12])[C:6]=2[C:13]=1[F:14]

参加物

10

反応物 7

HCID 14798Sodium HydroxideHCID 24243Trisodium PhosphateHCID 24437Sodium SulfiteHCID 2724126Tempo2 回HCID 23665760Sodium HypochloriteHCID 23668197Sodium Chlorite2 回HCID 579390212-(6,7-difluoro-1H-benzimidazol-1-yl)ethanol

生成物 1

HCID 57939018HCID 57939018、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6342Acetonitrile溶媒

反応条件

温度
42 °C

実験手順

2-(6,7-difluoro-1H-benzimidazol-1-yl)ethanol (2.96 g, 15 mmol) is taken into 75 ml of MeCN and sodium phosphate buffer (56 ml, 0.67 M, pH 6.8) and the mixture is heated to 42° C. TEMPO (165 mg, 1.05 mol) is added followed by the simultaneous dropwise addition of a solution of NaClO2 (3.38 g, 80% pure, 30 mmol in 15 ml water) and a solution of bleach (350 μL of 6% NaOCl in 7.5 mL water) over 1.5 hours. After 48 hrs, the same quantities of NaClO2 and bleach are added. After a further 24 hours, TEMPO (165 mg, 1.05 mol) is added and the reaction is stirred for 72 hrs. The darkened reaction is allowed to cool to room temperature followed by the dropwise addition of 30 ml of a saturated solution of Na2SO3 (exothermic). The reaction becomes almost colourless. Using 2 N NaOH, the pH is raised to 9.2 and the reaction is extracted 4 times with ethyl acetate. The pH is then lowered to 3.8 with 2 N HCl and the solution allowed to stand for 48 hours. 1.98 grams of white crystalline material is recovered. The mother liquor is reduced to half the volume and allowed to stand. A further 260 mg is collected. (Combined yield 2.23 g, 70%)

後処理

  1. waitAfter a further 24 hours
  2. customThe darkened reaction
  3. temperatureto cool to room temperature
  4. temperaturethe pH is raised to 9.2
  5. extractionthe reaction is extracted 4 times with ethyl acetate
  6. waitto stand for 48 hours
  7. custom1.98 grams of white crystalline material is recovered
  8. customA further 260 mg is collected

出典と根拠

ORDレコード
ord-30f47cbe4f4b43768cec6fba7773bde9
出典データセット
uspto-grants-2012_01
特許番号
US08093402B2

反応ノート

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