홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 736981
노트
인쇄 미리보기

반응식

HRID 736981 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

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

생성물 1

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

시약·촉매·용매 3

HCID 962Water
용매
HCID 8028Tetrahydrofuran용매3회
HCID 15413tert-Butyl methyl ether용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-45fcd5e380df4477a9bb78305c5d926f
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07595339B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트