Sodium Iodide → Methyl 4-(tetradecyloxy)benzoate

HRID 483557

Reaktionsgleichung

Reaktionsgleichung von HRID 483557
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.[CH2:12](Br)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+]>CC(C)=O>[CH2:25]([O:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:10][CH:11]=1)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH3:12]

Komponenten

6

Edukt 4

HCID 5238Sodium IodideHCID 7456MethylparabenHCID 8208Myristyl bromideHCID 11430Potassium Carbonate

Produkt 1

HCID 3312490Methyl 4-(tetradecyloxy)benzoateAusbeute 8,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

A well stirred mixture of 100 g of methyl 4-hydroxybenzoate, 182.25 g of tetradecylbromide, 136.26 g of potassium carbonate and 4.93 g of sodium iodide in 1-liter of acetone is refluxed for 48 hours. The mixture is poured into ice water, the solid collected and washed with water. The solid is dissolved in chloroform and washed with 1N sodium hydroxide, dried and evaporated to a residue which is crystallized from hexanes to give 18.5 g of the desired product as a white solid, m.p. 64°-66° C.

Aufarbeitung

  1. temperatureis refluxed for 48 hours
  2. customthe solid collected
  3. washwashed with water
  4. dissolutionThe solid is dissolved in chloroform
  5. washwashed with 1N sodium hydroxide
  6. customdried
  7. customevaporated to a residue which
  8. customis crystallized from hexanes

Quellen und Nachweise

ORD-Eintrag
ord-8b10c90479e647eab05f2001c902d059
Quelldatensatz
uspto-grants-1993_07
Patentnummer
US05225425

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