Acetone → HCID 4694880, Verbindung

HRID 1512778

Reaktionsgleichung

Reaktionsgleichung von HRID 1512778
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([OH:13])[C:11]=1[OH:12])[C:5]([O:7]C)=[O:6].C([O-])([O-])=O.[K+].[K+].Br[CH2:21][CH3:22].[CH3:23][C:24](C)=O>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([O:13][CH2:21][CH3:22])[C:11]=1[O:12][CH2:23][CH3:24])[C:5]([OH:7])=[O:6]

Komponenten

5

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of methyl 3-chloro-4,5-dihydroxybenzoate (D68) (1.0 g) in acetone (50 mL) stirred at room temp was added K2CO3 (6.9 g) and bromoethane (5.5 g). The reaction mixture was stirred at 60° C. for 18 h. After filteration, the filtrate was concentrated under reduced pressure. The residue was dissolved in tetrahydrofuran (20 mL) and methanol (20 mL), a solution of NaOH (1.0 g) in water (20 mL) was added to the above solution. The resulted mixture was stirred for 4 h and then the organic solvent was removed in vacuo. The aqueous layer was acidified with concentrated HCl to pH around 1. The solid was filtered and dried in vacuo to afford 3-chloro-4,5-bis(ethyloxy)benzoic acid (D69) (769 mg). δH (DMSO-d6, 400 MHz): 1.29 (3H, t), 1.36 (3H, t), 4.08-4.15 (4H, m), 7.46 (1H, d), 7.53 (1H, d), 13.16 (1H, br s). MS (ES): C11H13ClO4 requires 244; found 245.1 (M+H+).

Aufarbeitung

  1. concentrationAfter filteration, the filtrate was concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in tetrahydrofuran (20 mL)
  3. additionmethanol (20 mL), a solution of NaOH (1.0 g) in water (20 mL) was added to the above solution
  4. stirringThe resulted mixture was stirred for 4 h
  5. customthe organic solvent was removed in vacuo
  6. filtrationThe solid was filtered
  7. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-54fcef7f06c644c1884b7b24617130a0
Quelldatensatz
uspto-grants-2012_07
Patentnummer
US08217028B2

Verknüpfte Notizen

Wird geladen…