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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323517Erstellt: 25. Oktober 2026

1-Bromooctane → C8F17-O-(CF2)5H

https://huagongshe.com/reaction/323517

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BromooctaneHCID 8140—
EduktHexanediolHCID 147023—
EduktC8H17-O-(CH2)6-O-Coch3HCID 131722486—
EduktC8F17-O-(CF2)5CoohHCID 131722487—
ProduktC8F17-O-(CF2)5HHCID 131722485—

Reaktionsbedingungen

Temperatur185 °C

Reaktionsschritte

In a fashion similar to Example 8, hexanediol was alkylated with n-octyl bromide, the product was acetylated, and the resulting C8H17—O—(CH2)6—O—COCH3 was directly fluorinated and hydrolyzed as in Example 8 to C8F17—O—(CF2)5COOH, which was recrystallized from perfluorohexane. The recrystallized acid (37.5 g) was mixed with 4.0 g NaOH and 100 mL ethylene glycol and heated to 185° C. The product was washed with water, and the residual 27.9 g was distilled to give pure C8F17—O—(CF2)5H, micro b.p. 195° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06214253B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-885d695e1a67477aa0a5e02b06172446
Quellennotizuspto-grants-2001_04