StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Sodium borohydride → 4-Bromo-6-fluoro-2,3-dihydro-1H-inden-1-ol

HRID 574633
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 574633
[Br:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2=[O:12].[BH4-].[Na+]>C(O)C>[Br:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][CH:6]2[OH:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 4311764Sodium borohydrideHCID 117702304-bromo-6-fluoro-2,3-dihydro-1H-inden-1-one

Produkt 1

HCID 894444374-Bromo-6-fluoro-2,3-dihydro-1H-inden-1-olAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

According to Scheme 2, step 1: To a solution of 4-Bromo-6-fluoro-indan-1-one (10.0 g, 43.7 mmol) in ethanol (183 ml) at 0° C. NaBH4 (3.67 g, 97.0 mmol) was added in portions and then the mixture was stirred at room temperature for 18 h. After evaporation of solvents in vacuo, water was added to the residue, the solution was extracted 3 times with ethyl acetate, then 2N aqueous HCl was added and the combined organic layers were washed with saturated aq. NaHCO3 and water. After drying over Na2SO4 and filtration, solvents were evaporated in vacuo to give 10.0 g of 4-Bromo-6-fluoro-indan-1-ol (4a) which was used immediately in the next step without purification.

Aufarbeitung

  1. customat 0° C
  2. customAfter evaporation of solvents in vacuo, water
  3. additionwas added to the residue
  4. extractionthe solution was extracted 3 times with ethyl acetate
  5. addition2N aqueous HCl was added
  6. washthe combined organic layers were washed with saturated aq. NaHCO3 and water
  7. dry with materialAfter drying over Na2SO4 and filtration, solvents
  8. customwere evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d79fef12805943159f06ba839ae774d5
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09034897B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion