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Hydrogen Peroxide → HCID 69430334、化合物

HRID 1295510
ノート
印刷プレビュー

反応式

HRID 1295510 の反応式
[CH2:1]([N:8]1[CH2:14][CH:13]2[C:15]([C:17]3[CH:18]=[C:19]([CH:22]=[CH:23][CH:24]=3)[C:20]#[N:21])([OH:16])[CH:10]([CH2:11][CH2:12]2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-:26].[K+].[K+].OO>CS(C)=O>[CH2:1]([N:8]1[CH2:9][CH:10]2[C:15]([C:17]3[CH:18]=[C:19]([CH:22]=[CH:23][CH:24]=3)[C:20]([NH2:21])=[O:26])([OH:16])[CH:13]([CH2:12][CH2:11]2)[CH2:14]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=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 784Hydrogen PeroxideHCID 11430Potassium CarbonateHCID 69431388HCID 69431388、化合物

生成物 1

HCID 69430334HCID 69430334、化合物収率 570.8%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

3-(3-Benzyl-8-hydroxy-3-aza-bicyclo[3.2.1]oct-8-yl)-benzonitrile (1.86 g, 5.84 mmol) in DMSO (30 mL) with potassium carbonate (0.121 g, 0.88 mmol) was charged with 30% aqueous hydrogen peroxide (2.98 mL, 29.2 mmol) and allowed to stir at room temperature for 2 h (or until judged complete by TLC). The reaction was cooled in an ice bath then quenched with water (50 mL) causing the product precipitate as white solids. The mixture was acidified to pH 1 with 1N HCl (25 mL) to dissolve the product and the aqueous layer was washed with ether (2×30 mL). The ether extracts were back extracted with water (1×30 mL). The combined acidic aqueous layers were neutralized to pH 8 with saturated aqueous NaHCO3 solution. The product was extracted with EtOAc (3×50 mL), washed with 50% saturated aqueous NaCl solution (3×50 mL) then dried by azeotroping with THF (3×100 mL) yielding a white solid (1.69 g, 86%). 1H NMR (400 MHz, CD3OD) δ 7.96 (t, J=1.5 Hz, 1H), 7.95 (d, J=7.9 Hz, 1H), 7.64 (d, J=7.4 Hz, 1H), 7.41–7.15 (m, 6H), 3.56 (br s, 2H), 2.88 (m, 2H), 2.61 (m, 2H), 2.46 (br, s, 2H), 1.76 (m, 2H), 1.35 (m, 2H); APCI MS m/z 337.2 (M+1)+; mp 210–214° C.

後処理

  1. temperatureThe reaction was cooled in an ice bath
  2. customthen quenched with water (50 mL)
  3. dissolutionto dissolve the product
  4. washthe aqueous layer was washed with ether (2×30 mL)
  5. extractionThe ether extracts were back extracted with water (1×30 mL)
  6. extractionThe product was extracted with EtOAc (3×50 mL)
  7. washwashed with 50% saturated aqueous NaCl solution (3×50 mL)
  8. customthen dried
  9. customby azeotroping with THF (3×100 mL)

出典と根拠

ORDレコード
ord-72ec4c6520e8452fadd1d2cd7c0afdc6
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07241887B2

反応ノート

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