Reaktion #1605823

ord-5f1a7fe1eb294a49827aeb8e506e1f39

Reaktionsgleichung

COc1ccc(COc2ccc(C(=O)CBr)c3ccc(=O)[nH]c23)cc1
5-(2-bromoacetyl)-8-[(4-methoxyphenyl)methoxy]-1,2-dihydroquinolin-2-one
CO
methanol
COc1ccc(COc2ccc([C@@H](O)CBr)c3ccc(=O)[nH]c23)cc1
5-[(1R)-2-bromo-1-hydroxyethyl]-8-[(4-methoxyphenyl)methoxy]-1,2-dihydroquinolin-2-one
Ausbeute 42.5%

Reaktionsbedingungen

Temperatur
-20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was warmed gradually to 0° C
  2. 2
    Filtrationinsoluble matter was filtered off
  3. 3
    Waschenwashed with tetrahydrofuran
  4. 4
    workup.ADDITIONThe filtrate and the washing were mixed
  5. 5
    Einengenconcentrated under reduced pressure
  6. 6
    workup.ADDITIONTo the residue was added
  7. 7
    Sonstigepurified water (100 mL)
  8. 8
    workup.STIRRINGthe mixture was stirred at room temperature overnight
  9. 9
    FiltrationThe precipitate was collected by filtration
  10. 10
    Waschenwashed with purified water
  11. 11
    WaschenThe precipitate was further suspension-washed with ethyl acetate (200 mL)
  12. 12
    Filtrationcollected by filtration
  13. 13
    Sonstigedried under reduced pressure

Vorschrift

Under an argon flow, 5-(2-bromoacetyl)-8-[(4-methoxyphenyl)methoxy]-1,2-dihydroquinolin-2-one (7.15 g, 17.8 mmol) was suspended in dehydrated tetrahydrofuran (40 mL), the CBS catalyst (493 mg) was added thereto, and the reaction mixture was stirred at −20° C. for 40 minutes. After adding dropwise a 1.0 M solution of borane-tetrahydrofuran complex in tetrahydrofuran (21.4 mL) at the same temperature, the mixture was warmed gradually to 0° C. After adding methanol (20 mL) dropwise, insoluble matter was filtered off and washed with tetrahydrofuran. The filtrate and the washing were mixed and concentrated under reduced pressure. To the residue was added purified water (100 mL) and the mixture was stirred at room temperature overnight. The precipitate was collected by filtration and washed with purified water. The precipitate was further suspension-washed with ethyl acetate (200 mL), collected by filtration, and dried under reduced pressure to obtain 5-[(1R)-2-bromo-1-hydroxyethyl]-8-[(4-methoxyphenyl)methoxy]-1,2-dihydroquinolin-2-one (3.06 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09072734B2uspto-grants-2015_07