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Sodium Carbonate → 4-(3-Phenyl-indole-1-sulfonyl)-benzoic acid

HRID 736981
ノート
印刷プレビュー

反応式

HRID 736981 の反応式
C[O:2][C:3](=[O:23])[C:4]1[CH:9]=[CH:8][C:7]([S:10]([N:13]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:15](I)=[CH:14]2)(=[O:12])=[O:11])=[CH:6][CH:5]=1.[C:24]1(B(O)O)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C(=O)([O-])[O-].[Na+].[Na+].[OH-].[Na+]>C1COCC1.O.CC(OC)(C)C>[C:24]1([C:15]2[C:16]3[C:21](=[CH:20][CH:19]=[CH:18][CH:17]=3)[N:13]([S:10]([C:7]3[CH:8]=[CH:9][C:4]([C:3]([OH:2])=[O:23])=[CH:5][CH:6]=3)(=[O:11])=[O:12])[CH:14]=2)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 10340Sodium CarbonateHCID 14798Sodium HydroxideHCID 66827Phenylboronic AcidHCID 58974999Benzoic acid,4-[(3-iodo-1h-indol-1-yl)sulfonyl]-,methyl ester

生成物 1

HCID 589751414-(3-Phenyl-indole-1-sulfonyl)-benzoic acid

試薬・触媒・溶媒 3

HCID 962Water
溶媒
HCID 8028Tetrahydrofuran溶媒3 回
HCID 15413tert-Butyl methyl ether溶媒

実験手順

Add to a 2 L 3-neck flask equipped with reflux condenser, thermometer and nitrogen inlet, 4-(3-iodo-indole-1-sulfonyl)-benzoic acid methyl ester (0.1 mol, 44.1 g), phenylboronic acid (0.12 mol, 22.35 g), 1,1-bis(diphenylphosphino)ferrocene dichloropalladium (0.0025 mol, 2.04 g), 2M sodium carbonate (140 ml) and 0.5 L THF. Heat the mixture to reflux under nitrogen for 2 hours. Remove THF under vacuum, and add MTBE (500 ml) and DI water (200 ml) to the residue. Filter the solution through a pad of Celite, and wash with MTBE (500 ml). Separate the organic layer and concentrate under vacuum to give a brown solid. Dissolve the solid in THF (250 ml). Add to this solution 5N NaOH (35 ml) dropwise over a 30 minute period. Stir the reaction at ambient temperature for 3 hours, and quench with DI water (250 ml) and MTBE (250 ml). Separate the water layer and back extract the organic layer with DI water (250 ml). Combine the aqueous layers and wash with MTBE (500 ml). Stir the aqueous layer at ambient temperature and adjust the pH is to 1 with concentrated HCl. Stir the slurry at ambient temperature for 2 hours, filter and wash with DI water (500 ml). Dry the off-white, gray solid in vacuum oven at 65° C. for 16 hours to obtain 25.44 g. 1H NMR (DMSO) 8.2 (d, 2H), 8.1 (m, 3H), 7.9 (d, 1H), 7.7 (d, 2H), 7.4 (m, 5H). MS (ES−)=376.2 (M−1). Anal. Calcd. For C21H15NO4S: C, 66.8308; H, 4.0060; N, 3.7112. found C, 66.54; H, 4.07; N, 3.20.

後処理

  1. additionAdd to a 2 L 3-neck flask
  2. customequipped
  3. temperaturewith reflux condenser
  4. temperatureHeat the mixture
  5. temperatureto reflux under nitrogen for 2 hours
  6. filtrationFilter the solution through a pad of Celite
  7. washwash with MTBE (500 ml)
  8. customSeparate the organic layer
  9. concentrationconcentrate under vacuum
  10. customto give a brown solid
  11. customthe reaction at ambient temperature for 3 hours
  12. customquench with DI water (250 ml) and MTBE (250 ml)
  13. customSeparate the water layer
  14. extractionback extract the organic layer with DI water (250 ml)
  15. washCombine the aqueous layers and wash with MTBE (500 ml)
  16. stirringStir the aqueous layer at ambient temperature
  17. stirringStir the slurry at ambient temperature for 2 hours
  18. filtrationfilter
  19. washwash with DI water (500 ml)
  20. customDry the off-white, gray solid in vacuum oven at 65° C. for 16 hours
  21. customto obtain 25.44 g

出典と根拠

ORDレコード
ord-45fcd5e380df4477a9bb78305c5d926f
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07595339B2

反応ノート

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