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Citric Acid → 2-[2-[4-[((3S)-1-acetyl-3-pyrrolidinyl)oxy]-3-hydroxyphenyl]vinyl]-5-benzofurancarbonitrile

HRID 361930
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 361930
C([O:4][C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][C:12]=1[O:13][C@H:14]1[CH2:18][CH2:17][N:16]([C:19](=[O:21])[CH3:20])[CH2:15]1)[CH:8]=O)(=O)C.[Cl-].[C:23]([C:25]1[CH:26]=[CH:27][C:28]2[O:32][C:31]([CH2:33][P+](C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)=[CH:30][C:29]=2[CH:53]=1)#[N:24].C1CCN2C(=NCCC2)CC1.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>O1CCCC1.C(O)C.O>[C:19]([N:16]1[CH2:17][CH2:18][C@H:14]([O:13][C:12]2[CH:11]=[CH:10][C:7]([CH:8]=[CH:33][C:31]3[O:32][C:28]4[CH:27]=[CH:26][C:25]([C:23]#[N:24])=[CH:53][C:29]=4[CH:30]=3)=[CH:6][C:5]=2[OH:4])[CH2:15]1)(=[O:21])[CH3:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 311Citric AcidHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene2×HCID 21844326(5-Cyano-2-benzofuranyl)methyltriphenylphosphonium chlorideHCID 571530353-acetyloxy-4-[((3S)-1-acetyl-3-pyrrolidinyl)oxy]benzaldehyde

Produkt 1

HCID 570808862-[2-[4-[((3S)-1-acetyl-3-pyrrolidinyl)oxy]-3-hydroxyphenyl]vinyl]-5-benzofurancarbonitrile
Ausbeute 103,8 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

1.3 g of 3-acetyloxy-4-[((3S)-1-acetyl-3-pyrrolidinyl)oxy]benzaldehyde and 2.22 g of (5-cyano-2-benzofuranyl)methyltriphenylphosphonium chloride were dissolved in a solvent mixture of 10 ml of tetrahydrofuran and 10 ml of ethanol, followed by the addition of 0.943 g of 1,8-diazabicyclo[5.4.0]-7-undecene and by subsequent stirring at room temperature for 2 hours. To the mixture obtained were further added 1.88 g of 1,8-diazabicyclo[5.4.0]-7-undecene and 3 ml of water, followed by stirring at room temperature for 2 hours. The thus prepared reaction solution was adjusted to pH 4-5 with 10% citric acid aqueous solution and concentrated under a reduced pressure, and the resulting residue was extracted with chloroform, and then dried. After distilling off the solvent, the resulting residue was purified by subjecting it to silica gel column chromatography using a chloroform/ethanol mixture as an elution solvent, thereby obtaining 1.8 g of 2-[2-[4-[((3S)-1-acetyl-3-pyrrolidinyl)oxy]-3-hydroxyphenyl]vinyl]-5-benzofurancarbonitrile as a powdery mixture of E and Z forms.

Aufarbeitung

  1. customTo the mixture obtained
  2. stirringby stirring at room temperature for 2 hours
  3. customThe thus prepared reaction solution
  4. concentrationconcentrated under a reduced pressure
  5. extractionthe resulting residue was extracted with chloroform
  6. customdried
  7. distillationAfter distilling off the solvent
  8. customthe resulting residue was purified

Quellen und Nachweise

ORD-Eintrag
ord-eb56c0c9605745e2b9e5f251dbdf03bf
Quelldatensatz
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05866577

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