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Methyl iodide → Methyl 2,2'-dichlorobenzilate

HRID 1994211
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1994211
[Cl:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[C:4]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[Cl:15])([OH:8])[C:5]([OH:7])=[O:6].[O-][CH2:21]C.[Na+].[Na].CI>C(O)C.O>[Cl:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[C:4]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[Cl:15])([OH:8])[C:5]([O:7][CH3:21])=[O:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 6328Methyl iodideHCID 3290602,2'-Dichlorobenzilic acidHCID 2723922Sodium ethoxideHCID 5360545Sodium

Produkt 1

HCID 22574193Methyl 2,2'-dichlorobenzilate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittel2×
HCID 962WaterLösungsmittel

Versuchsvorschrift

A solution of 10.0 g (0.034 mol) of 2,2′-dichlorobenzilic acid in 50 ml of ethanol was added dropwise to freshly prepared sodium ethoxide solution of 0.78 g (0.034 mol) of sodium and 100 ml of ethanol at 20° C. and stirred overnight. The solution was evaporated to dryness, the residue was dissolved in DMF and at 20° C. 9.57 g (0.0674 mol) of methyl iodide were added dropwise and the mixture was stirred for a further 72 hours. 300 ml of water were added dropwise to the resulting suspension while cooling with ice, it was extracted with diethyl ether, the organic phase was washed with water, dried over Na2SO4, and evaporated to dryness. Yield: 10.48 g (100% of theory).

Aufarbeitung

  1. customThe solution was evaporated to dryness
  2. dissolutionthe residue was dissolved in DMF and at 20° C
  3. stirringthe mixture was stirred for a further 72 hours
  4. temperaturewhile cooling with ice, it
  5. extractionwas extracted with diethyl ether
  6. washthe organic phase was washed with water
  7. dry with materialdried over Na2SO4
  8. customevaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-5981b5f934ff40f2a05b76d0adb4853e
Quelldatensatz
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07652138B2

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