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Lithium Hydroxide → 8-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acid

HRID 642836
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 642836
[Li+].[OH-].[CH3:3][C:4]1[C:9]2[O:10][CH2:11][CH2:12][O:13][C:8]=2[CH:7]=[C:6]([C:14]([O:16]C)=[O:15])[CH:5]=1.[OH-].[Na+]>O.C1COCC1>[CH3:3][C:4]1[C:9]2[O:10][CH2:11][CH2:12][O:13][C:8]=2[CH:7]=[C:6]([C:14]([OH:16])=[O:15])[CH:5]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 3939Lithium HydroxideHCID 14798Sodium HydroxideHCID 45122025Methyl 8-methyl-2,3-dihydro-1,4-benzodioxin-6-carboxylate

Produkt 1

HCID 451220248-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel
HCID 8028
Tetrahydrofuran
Lösungsmittel

Versuchsvorschrift

A solution of 6.65 g (0.28 mol) LiOH in 100 mL water was metered into a solution of 33.60 g (0.16 mol) methyl 8-methyl-2,3-dihydro-1,4-benzodioxin-6-carboxylate in 200 mL THF and the reaction solution was stirred overnight at RT. To complete the reaction 150 mL 6 M NaOH were added and the mixture was stirred for a further 2 h at 50° C. The reaction mixture was evaporated down i.vac, the residue was combined with THF, acidified with conc. HCl while cooling with ice, the precipitate was filtered off, washed with 150 mL water and dried at 60° C. in the circulating air dryer.

Aufarbeitung

  1. additionwere added
  2. stirringthe mixture was stirred for a further 2 h at 50° C
  3. customThe reaction mixture was evaporated down i.vac
  4. temperaturewhile cooling with ice
  5. filtrationthe precipitate was filtered off
  6. washwashed with 150 mL water
  7. customdried at 60° C. in the circulating air dryer

Quellen und Nachweise

ORD-Eintrag
ord-5b61e9b4be5a420c8cd3368b8cc611f6
Quelldatensatz
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07696195B2

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