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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733196Generated: October 26, 2026

Hexachlorocyclopentadiene → 1,2,3,4,9,9-Hexachloro-1,4,4a,5,6,7,8,8a-octahydro-1,4-methanonaphthalene-6-carbonitrile

https://huagongshe.com/reaction/1733196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachlorocyclopentadieneHCID 6478—
Reactant3-Cyclohexene-1-carbonitrileHCID 66013—
Product1,2,3,4,9,9-Hexachloro-1,4,4a,5,6,7,8,8a-octahydro-1,4-methanonaphthalene-6-carbonitrileHCID 20300612—

Reaction Steps

3-Cyclohexene-1-carbonitrile (Aldrich Chemical Corp.) (56 g.), and 200 g. of hexachlorocyclopentadiene were mixed, heated at 160°-170° C. for 6 hours, and then allowed to cool to room temperature. The reaction mixture was then vacuum distilled. Unreacted hexachlorocyclopentadiene was first removed and then the crude adduct produced was collected, 175°-170° C. at 0.3 m.m. Hg. The thick liquid was crystallized very slowly in Skelly "B". The crude solid melted at 140°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04240974
Source datasetuspto-grants-1980_12
ORD IDord-e63adf911250485a8907392ad25f5221
Source noteuspto-grants-1980_12