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Hydrochloric Acid → 2,6-Bis(2-carboxyethyl)naphthalene

HRID 2371551
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2371551
[Na].[C:2]([O:10]CC)(=[O:9])[CH2:3][C:4](OCC)=O.BrC[C:15]1[CH:24]=[CH:23][C:22]2[C:17](=[CH:18][CH:19]=[C:20]([CH2:25]Br)[CH:21]=2)[CH:16]=1.Cl>C(O)C>[C:2]([CH2:3][CH2:25][C:20]1[CH:19]=[CH:18][C:17]2[C:22](=[CH:23][CH:24]=[C:15]([CH2:4][CH2:3][C:2]([OH:10])=[O:9])[CH:16]=2)[CH:21]=1)([OH:10])=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 7761Diethyl MalonateHCID 36600102,6-Bis(bromomethyl)naphthaleneHCID 5360545Sodium

Produkt 1

HCID 199073652,6-Bis(2-carboxyethyl)naphthaleneAusbeute 265,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702
Ethanol
Lösungsmittel

Versuchsvorschrift

First, 228 mg of metallic sodium was dissolved in 10 ml of absolute ethanol, and after adding 3.02 g of diethyl malenate, the mixture was refluxed for 5 minutes and cooled. After adding 504 mg of diethyl malonate and then 1.41 g of 2,6-bis(bromomethyl)naphthalene at once, the mixture was refluxed 2 hours. After cooling and adding 20 ml of ice water, the reaction mixture was adjusted to pH 6.0 with 1N hydrochloric acid and extracted twice with 100 ml of benzene. The extracts were combined, washed with water and a saturated sodium chloride aqueous solution, dried over magnesium sulfate, filtered, and evaporated under a reduced pressure. To the resulting pale yellow oil were added 15 ml of acetic acid and 15 ml of concentrated hydrochloric acid, and the mixture was refluxed for 23 hours, cooled and concentrated. After adding 5 ml of water, the resulting crystal was collected by filtration, washed with water and dried in air and then under a reduced pressure to obtain 1.136 g of the title compound as colorless crystal.

Aufarbeitung

  1. temperaturethe mixture was refluxed for 5 minutes
  2. temperaturecooled
  3. temperatureAfter cooling
  4. extractionextracted twice with 100 ml of benzene
  5. washwashed with water
  6. dry with materiala saturated sodium chloride aqueous solution, dried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated under a reduced pressure
  9. additionTo the resulting pale yellow oil were added 15 ml of acetic acid and 15 ml of concentrated hydrochloric acid
  10. temperaturethe mixture was refluxed for 23 hours
  11. temperaturecooled
  12. concentrationconcentrated
  13. additionAfter adding 5 ml of water
  14. filtrationthe resulting crystal was collected by filtration
  15. washwashed with water
  16. customdried in air

Quellen und Nachweise

ORD-Eintrag
ord-9bb0e7ffd3ac46ae8f562904bd058278
Quelldatensatz
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05093370

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