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HRID 46691Erstellt: 24. Oktober 2026

Acetic Acid → 1,2,3,4,9,9-Hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione

https://huagongshe.com/de/reaction/46691

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktWaterHCID 962—
Edukt1,2,3,4,9,9-Hexachloro-1,4,4A,8A-tetrahydro-1,4-methanonaphthalene-5,8-dioneHCID 228947—
KatalysatorZincHCID 23994—
LösungsmittelChloroformHCID 6212—
Produkt1,2,3,4,9,9-Hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dioneHCID 20300594—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

38 g. of 1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4-methanonaphthalene-5,8-dione, prepared as in Example 1, were suspended in 150 ml. of glacial acetic acid and then this mixture was poured into 20 g. of zinc dust suspended in 150 ml. of distilled water. A slight exotherm occurred during stirring and the temperature was maintained at 50° C. for 3 hours by external heating. Then 200 ml. of chloroform were added and stirring was continued for 30 minutes more. The chloroform layer was separated and washed with a saturated sodium carbonate solution and dried over anhydrous magnesium sulfate. Evaporation of the chloroform left a white solid. One recrystallization from methanol gave white crystals, m.p. 169°-170° C. Infrared spectrum showed carbonyl at 1740 cm-1. The nmr indicated two bridgehead protons at 431 Hz (singlet) and four α-protons at 303 Hz and 245 Hz (as a multiplet).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04174457
Quelldatensatzuspto-grants-1979_11
ORD IDord-53f029cbc50d4263a98ea3b05e2cea99
Quellennotizuspto-grants-1979_11