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Trimethyl borate → (2-Methoxy-3-nitrophenyl)methanol

HRID 1861956
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1861956
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([N+:10]([O-:12])=[O:11])[C:5]=1[O:13][CH3:14].[BH4-].[Li+].B(OC)(OC)OC>O1CCCC1>[CH3:14][O:13][C:5]1[C:6]([N+:10]([O-:12])=[O:11])=[CH:7][CH:8]=[CH:9][C:4]=1[CH2:3][OH:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8470Trimethyl borateHCID 590805Methyl 2-methoxy-3-nitrobenzoateHCID 4148881Lithium borohydride

Produkt 1

HCID 18789679(2-Methoxy-3-nitrophenyl)methanolAusbeute 76,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A mixture of 2-methoxy-3-nitrobenzoic acid methyl ester (4.82 g), lithium borohydride (298 mg), trimethyl borate (0.27 ml) and anhydrous tetrahydrofuran (200 ml) was heated under reflux for 5 h. The reaction mixture was distilled under reduced pressure and ethyl acetate and water were added to the resulting residue. The organic layer was washed with a saturated aqueous sodium chloride solution, dried with anhydrous sodium sulfate and distilled under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=1:1) to give 3.18 g of the titled compound (yield, 76%).

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 5 h
  3. distillationThe reaction mixture was distilled under reduced pressure and ethyl acetate and water
  4. additionwere added to the resulting residue
  5. washThe organic layer was washed with a saturated aqueous sodium chloride solution
  6. dry with materialdried with anhydrous sodium sulfate
  7. distillationdistilled under reduced pressure
  8. customThe resulting residue was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=1:1)

Quellen und Nachweise

ORD-Eintrag
ord-b7f432aefc3d4a9da316f54fa294f86b
Quelldatensatz
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06534546B1

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