Monobasic potassium phosphate → 7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptanoic acid

HRID 1443650Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1443650
Cl[O-].[Na+].[CH3:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[N:13]=[C:14]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH:23]=[O:24])[S:15][CH:16]=2)=[CH:8][CH:7]=1.P([O-])(O)(O)=[O:26].[K+]>C(O)(C)(C)C.O.C(OCC)(=O)C>[CH3:4][O:5][C:6]1[CH:7]=[CH:8][C:9]([C:12]2[N:13]=[C:14]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][C:23]([OH:26])=[O:24])[S:15][CH:16]=2)=[CH:10][CH:11]=1

Komponenten

7

Versuchsvorschrift

Add 2-methyl-27-butene (7.0 mL) and sodium hypochlorite (2.51 g, 27.75 mmol) to a solution of 7-[4-(4-methoxyphenyl)thiazol-2-yl]heptanal (4.02 g, 13.25 mmol) and potassium dihydrogen phosphate (3.10 g, 22.78 mmol) in tert-butanol (60 mL) and water (12 mL) at room temperature. Stir the mixture for 40 minutes, dilute with ethyl acetate (500 mL) and wash with brine (3×200 mL). Dry the combined organic extracts over sodium sulfate and remove the solvent under reduced pressure. Purify the residue by flash column chromatography on silica gel, eluting with methanol/methylene chloride (1:19), and triturate the residue with hexanes/methylene chloride to afford 7-[4-(4-methoxyphenyl)thiazol-2-yl]heptanoic acid (3.91 g, 88%): APCI MS m/z 320 [C17H21NO3S+H]+.

Aufarbeitung

  1. washwash with brine (3×200 mL)
  2. dry with materialDry the combined organic extracts over sodium sulfate
  3. customremove the solvent under reduced pressure
  4. customPurify the residue by flash column chromatography on silica gel
  5. washeluting with methanol/methylene chloride (1:19)
  6. customtriturate the residue with hexanes/methylene chloride

Quellen und Nachweise

ORD-Eintrag
ord-e1866ce6c2e84914a47d010d14876ffa
Quelldatensatz
uspto-grants-2010_02
Patentnummer
US07662771B2

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