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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7330Erstellt: 24. Oktober 2026

Ethylparaben → 4-[4-[(3-Ethyl-3-oxetanyl)methoxy]butoxy]benzoic acid

https://huagongshe.com/de/reaction/7330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylparabenHCID 8434—
Edukt3-[(4-Bromobutoxy)methyl]-3-ethyloxetaneHCID 21989315—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[4-[(3-Ethyl-3-oxetanyl)methoxy]butoxy]benzoic acidHCID 2196062890,3%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

In a 300 ml three neck flask, 5.2 g (31 mmol) of ethyl p-hydroxybenzoate, 4.7 g (34 mmol) of potassium carbonate anhydride, and 7.8 g (31 mmol) of the 3-[(4-bromobutoxy)methyl]-3-ethyloxetane were dissolved in 50 ml of dimethylformamide. After the solution remained turbid was heated to a temperature of 80° C. and stirred for 4 hours, the solvent was completely distilled out in a vacuum. To the resulting yellow oily substance were added 15 ml of a 7% sodium hydroxide aqueous solution and 15 ml of methanol. The mixture was refluxed for two and half hours. 1 N (normality) of hydrochloric acid was added to the mixture such that the pH is adjusted to about 3. The resulting white precipitate was filtered and dried in a vacuum thereby obtaining 8.6 g (28 mmol) of 4-[7-(3-ethyl-3-oxetanyl)-1,6-dioxaheptyl]benzoic acid (yield: 89%, identified with 1H-NMR). The resulting compound was no more purified and used in the following reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087273B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-e20a963324004b499bf87587735aa884
Quellennotizuspto-grants-2006_08