Methanol → HCID 69206248, Verbindung

HRID 2220102Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2220102
[CH2:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]2[CH:11]=[C:12](OS(C(F)(F)F)(=O)=O)[CH:13]=[CH:14][CH:15]=2)[CH2:6][CH2:5]1)[CH2:2][CH3:3].[CH2:24](N(CC)CC)C.[CH3:31][OH:32].[OH2:33]>CS(C)=O.CC([O-])=O.CC([O-])=O.[Pd+2].C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:31][O:32][C:24](=[O:33])[C:12]1[CH:13]=[CH:14][CH:15]=[C:10]([CH:7]2[CH2:8][CH2:9][N:4]([CH2:1][CH2:2][CH3:3])[CH2:5][CH2:6]2)[CH:11]=1

Komponenten

8

Edukt 4

HCID 887MethanolHCID 962WaterHCID 8471TriethylamineHCID 12988960HCID 12988960, Verbindung

Produkt 1

HCID 69206248HCID 69206248, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 812191,3-Bis(diphenylphosphino)propaneKatalysatorHCID 167845palladium(II) acetateKatalysatorHCID 679Dimethyl SulfoxideLösungsmittel

Versuchsvorschrift

A mixture of trifluoro-methanesulfonic acid 3-(1-propyl-piperidin-4-yl)-phenyl ester (1.2 g), triethyl amine (0.9 g), MeOH (5.4 ml), Pd(OAc)2 (25 mg) and 1,3-bis(di-phenyl-phosphino)propane (45 mg) in 15 ml DMSO was stirred at room temperature for 15 min. A stream of CO (g) was passed through the solution for 4-5 min., and then the reaction vessel was placed under a sligthly positive pressure of CO (g). The temp was increased to 70° C. After 6 h the reaction was allowed to cool to r.t. Water was then added, and the aqueous solution was extracted with five portions of ethyl acetate and the combined organic phases were dried (MgSO4), and evaporated. The residue was chromathographed on a silica column using MeOH:CH2Cl2 (1:9 (v/v)) as eluent. The fractions containing pure titled compound were collected, and the solvent was removed in vacuum, affording 650 mg of the titled compound. (MS m/z (rel. intensity, 70 eV) 261 (M+, 5), 233 (16), 232 (bp), 161 (5), 70 (20)

Aufarbeitung

  1. waitA stream of CO (g) was passed through the solution for 4-5 min.
  2. temperatureThe temp was increased to 70° C
  3. waitAfter 6 h the reaction was allowed
  4. temperatureto cool to r.t
  5. extractionthe aqueous solution was extracted with five portions of ethyl acetate
  6. dry with materialthe combined organic phases were dried (MgSO4)
  7. customevaporated
  8. additionThe fractions containing pure titled compound
  9. customwere collected
  10. customthe solvent was removed in vacuum

Quellen und Nachweise

ORD-Eintrag
ord-e7f296e4e15f462e8579733b01e31034
Quelldatensatz
uspto-grants-2008_08
Patentnummer
US07417043B2

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