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Nitronium tetrafluoroborate → trans-3,4-Dihydro-2,2-dimethyl-4-(1-oxoisoindolin-2-yl)-6-trifluoromethylsulfonyl-2H-1-benzopyran-3-yl nitrate

HRID 1656456
Notizen
Druckvorschau

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Reaktionsgleichung von HRID 1656456
F[B-](F)(F)F.[O:6]=[N+:7]=[O:8].[CH3:9][C:10]1([CH3:38])[C@@H:15]([OH:16])[C@H:14]([N:17]2[CH2:25][C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:18]2=[O:26])[C:13]2[CH:27]=[C:28]([S:31]([C:34]([F:37])([F:36])[F:35])(=[O:33])=[O:32])[CH:29]=[CH:30][C:12]=2[O:11]1>C(Cl)Cl.O>[N+:7]([O-:8])([O:16][C@H:15]1[C@H:14]([N:17]2[CH2:25][C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:18]2=[O:26])[C:13]2[CH:27]=[C:28]([S:31]([C:34]([F:37])([F:35])[F:36])(=[O:33])=[O:32])[CH:29]=[CH:30][C:12]=2[O:11][C:10]1([CH3:38])[CH3:9])=[O:6]
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Komponenten

5

Edukt 2

HCID 11073463Nitronium tetrafluoroborateHCID 14748246trans-3,4-Dihydro 2,2-dimethyl-4-(1-oxoisoindolin-2-yl)-6-trifluoromethylsulfonyl-2H-1-benzopyran-3-ol

Produkt 1

HCID 67859320trans-3,4-Dihydro-2,2-dimethyl-4-(1-oxoisoindolin-2-yl)-6-trifluoromethylsulfonyl-2H-1-benzopyran-3-yl nitrateAusbeute 26,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel
HCID 6344
Dichloromethane
Lösungsmittel

Versuchsvorschrift

116 mg of nitronium tetrafluoroborate were added to a solution of 300 mg of trans-3,4-dihydro-2,2-dimethyl-4-(1-oxoisoindolin-2-yl)-6-trifluoromethylsulfonyl-2H-1-benzopyran-3-ol (prepared as described in Preparation 13) in 5 ml of methylene chloride, and the resulting mixture was stirred at room temperature for 1.5 hours. At the end of this time, the reaction mixture was diluted with 20 ml of water and extracted with 15 ml of methylene chloride. The extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using a 1:4 by volume mixture of ethyl acetate and cyclohexane as the eluent, to afford 88 mg of the title compound as crystals, melting at 189.5°-190° C.

Aufarbeitung

  1. extractionextracted with 15 ml of methylene chloride
  2. washThe extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order
  3. dry with materialafter which it was dried over anhydrous magnesium sulfate
  4. customThe solvent was then removed by distillation under reduced pressure
  5. customthe resulting residue was purified by column chromatography through silica gel
  6. additionby volume mixture of ethyl acetate and cyclohexane as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-7c14f7ec756c4d5e977b765c36ee4f43
Quelldatensatz
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05254578

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