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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 259218Erstellt: 25. Oktober 2026

1,3-Dinitrobenzene → 3-Fluoro-1-trifluoroacetoxyadamantane

https://huagongshe.com/reaction/259218

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DinitrobenzeneHCID 7452—
EduktHypofluorous acid, trifluoromethyl esterHCID 78989—
Edukt1-Adamantyl trifluoroacetateHCID 10879458—
LösungsmittelTrichlorofluoromethaneHCID 6389—
Produkt3-Fluoro-1-trifluoroacetoxyadamantaneHCID 5397829445,9%

Reaktionsschritte

A solution of 1-trifluoroacetoxyadamantane (1.0 g, 4.0 mmole, prepared by reacting adamantan-1-ol with trifluoroacetic anhydride in dry pyridine) in fluorotrichloromethane (10 ml), containing m-dinitrobenzene (80 mg, 0.48 mmole), was treated with trifluoromethyl hypofluorite (4.5 mmole) at -25° for 24 hours, air being recrystallization admitted to the reaction vessel during this time. The product was recovered in a similar manner to that described in Example 3 and was chromatographed on silica (100 g). Elution with chloroform:hexane (1:5) afforded unreacted starting material (152 mg), while elution with chloroform:hexane (1:4) gave liquid 3-fluoro-1-trifluoroacetoxyadamantane (489 mg) which appeared homogeneous by g.l.c. This product sublimed at 70° (bath)/1 mm Hg to give a crystalline solid m.p. 28°-32°; νmax (film) 1780 cm-1 ; PMR 1.5-2.6 (m, adamantyl protons); FMR φ* + 76.2 (s, CF3COO--) and + 133.5 (broad s) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04036864
Quelldatensatzuspto-grants-1977_07
ORD IDord-f478b0e1373841798450be81f71acaf8
Quellennotizuspto-grants-1977_07