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Ethanol → 1-Naphthol

HRID 1867247
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1867247
[C:1]1([O:11]C2C3C(=CC=CC=3)C=CC=2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.B(Br)(Br)Br.C(O)C.C([O-])(O)=O.[Na+]>C(Cl)Cl>[CH:7]1[CH:8]=[CH:9][C:10]2[C:5](=[CH:4][CH:3]=[CH:2][C:1]=2[OH:11])[CH:6]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 702EthanolHCID 25134Boron tribromideHCID 2356111-Naphthyl etherHCID 516892Sodium Bicarbonate

Produkt 1

HCID 70051-NaphtholAusbeute 94,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
-70 °C

Versuchsvorschrift

Naphthylether 10 (19.8 g, 81 mmol) was dissolved in a dry DCM (400 mL) and the solution cooled to −70° C. A solution of BBr3 (1M in DCM, 160 mL, 160 mmol) was added dropwise while maintaining an internal temperature below −60° C. The mixture was aged at this temperature for an additional 30 min, then allowed to warm up to RT and aged for additional 2 h at rt. The mixture was then again cooled to −70° C., treated with absolute ethanol (20 mL), and the resulting mixture was aged at rt overnight. The solution was poured into a cold NaHCO3 solution (500 mL, saturated aq) and vigorously stirred. The organic layer was washed with dilute HCl solution (0.1N, 200 mL) and with water (200 mL), and the solvent removed. Column chromatography of the resulting residue using 20% ethyl acetate in hexanes yielded the naphthylester 12 (17.6 g, 76.4 mmol) in 94% yield.

Aufarbeitung

  1. temperaturewhile maintaining an internal temperature below −60° C
  2. temperatureto warm up to RT
  3. waitaged for additional 2 h at rt
  4. temperatureThe mixture was then again cooled to −70° C.
  5. waitthe resulting mixture was aged at rt overnight
  6. washThe organic layer was washed with dilute HCl solution (0.1N, 200 mL) and with water (200 mL)
  7. customthe solvent removed

Quellen und Nachweise

ORD-Eintrag
ord-c6cd9d6621fc45449f88b90e427e0bc1
Quelldatensatz
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07632828B2

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