Water → 6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one

HRID 971272Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 971272
F[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[CH2:7][CH2:6][CH2:5]2.[C:13]1([SH:19])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C([O-])([O-])=O.[K+].[K+].O>CN1CCCC1=O.CCOC(C)=O>[C:13]1([S:19][C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[C:8](=[O:12])[CH2:7][CH2:6][CH2:5]3)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Komponenten

7

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A solution of 6-fluoro-3,4-dihydro-2H-naphthalen-1-one (5.51 g, 33.56 mmol), benzenethiol (4.07 g, 3.79 mL, 36.92 mmol) and K2CO3 (9.28 g, 67.12 mmol) in 50 mL of N-methylpyrrolidinone (NMP) was heated to 80° C. under argon and stirred at 80° C. for 2 hours. The reaction mixture was poured int 500 mL of water and diluted with 300 mL of EtOAc. The layers were separated and the aqueous layer was extracted twice with 250 mL of EtOAc. The combinded organic layers were washed with water, saturated brine, and then dried over MgSO4. The solvent was removed under reduced pressure to yield an oil which was eluted through silica gel using hexanes/EtOAc (9:1). Removal of solvent under reduced pressure provided 8.05 g (31.65 mmol, 94.31%) of 6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one as a pale yellow oil. MS: 255 (M+H)+.

Aufarbeitung

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted twice with 250 mL of EtOAc
  3. washThe combinded organic layers were washed with water, saturated brine
  4. dry with materialdried over MgSO4
  5. customThe solvent was removed under reduced pressure
  6. customto yield an oil which
  7. washwas eluted through silica gel
  8. customRemoval of solvent under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-7c866dd811394de3896b1618089db879
Quelldatensatz
uspto-grants-2007_12
Patentnummer
US07312359B2

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