Carbon Dioxide → 5-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acid

HRID 1768665Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1768665
Br[C:2]1[CH:11]=[CH:10][C:5]2[O:6][CH2:7][CH2:8][O:9][C:4]=2[C:3]=1[CH3:12].C([Li])CCC.[C:18](=[O:20])=[O:19].O>O1CCCC1>[CH3:12][C:3]1[C:4]2[O:9][CH2:8][CH2:7][O:6][C:5]=2[CH:10]=[CH:11][C:2]=1[C:18]([OH:20])=[O:19]

Komponenten

6

Edukt 4

HCID 280Carbon Dioxide2×HCID 962WaterHCID 124645276-Bromo-5-methyl-2,3-dihydro-1,4-benzodioxineHCID 178418339Butyllithium

Produkt 1

HCID 107029595-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acidAusbeute 77 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

In 300 ml of dry tetrahydrofuran, was dissolved 32.0 g of 6-bromo-5-methyl-1,4-benzodioxane and after cooling the solution to -78° C., 96.7 ml of n-butyl lithium (n-hexane solution) was added dropwise over 20 minutes or more. After stirring at the same temperature for 1.5 hours, the reaction mixture was poured onto crushed dry ice and dry ice was sublimated while stirring. Water was added to the mixture and the tetrahydrofuran was removed under reduced pressure. The resulting alkaline aqueous solution was washed with methylene chloride and adjusted to pH 3 with a 5% hydrochloric acid, and the precipitated crystals were collected by filtration and dried to obtain 20.9 g of 5-methyl-1, 4-benzodioxan-6-carboxylic acid (yield: 77%).

Aufarbeitung

  1. additionthe reaction mixture was poured
  2. stirringwhile stirring
  3. customthe tetrahydrofuran was removed under reduced pressure
  4. washThe resulting alkaline aqueous solution was washed with methylene chloride
  5. filtrationthe precipitated crystals were collected by filtration
  6. customdried

Quellen und Nachweise

ORD-Eintrag
ord-d078251872f448e7b8f5d22637e8a05c
Quelldatensatz
uspto-grants-1995_01
Patentnummer
US05378726

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