Hydrochloric Acid → (2,6-Dimethyl-3-nitrophenyl)methanol

HRID 613603

Reaktionsgleichung

Reaktionsgleichung von HRID 613603
[CH3:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[C:7]([CH3:14])[C:3]=1[C:4](O)=[O:5].Cl>O1CCCC1>[CH3:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[C:7]([CH3:14])[C:3]=1[CH2:4][OH:5]

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 2393292,6-Dimethyl-3-nitrobenzoic acid

Produkt 1

HCID 10487641(2,6-Dimethyl-3-nitrophenyl)methanolAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 2,6-dimethyl-3-nitrobenzoic acid (3.09 g) in tetrahydrofuran (5 ml) was added borane-methyl sulfide complex (2.41 g) under ice-cooling, and the mixture was stirred for 30 minutes at the same temperature, for 1 hour at ambient temperature, and then for 4 hours under heating. To the mixture was added 1N hydrochloric acid under ice-cooling, and the mixture was allowed to stand overnight. The mixture was extracted with ethyl acetate twice, and the combined organic layer was washed with saturated sodium bicarbonate solution, water and brine, dried over magnesium sulfate and concentrated. The residue was recrystallized with diisopropyl ether to give 2,6- dimethyl-3-nitrobenzyl alcohol (2.296 g) as a pale yellow crystal.

Aufarbeitung

  1. temperaturecooling
  2. temperaturefor 4 hours under heating
  3. temperaturecooling
  4. waitto stand overnight
  5. extractionThe mixture was extracted with ethyl acetate twice
  6. washthe combined organic layer was washed with saturated sodium bicarbonate solution, water and brine
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated
  9. customThe residue was recrystallized with diisopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-fd7df1b41bf74427a9876cc7b1342632
Quelldatensatz
uspto-grants-1999_12
Patentnummer
US06008229

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