HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexachlorocyclopentadiene → 1,2,3,4,9,9-Hexachloro-1,4,4a,5,6,7,8,8a-octahydro-1,4-methanonaphthalene-6-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexachlorocyclopentadiene | HCID 6478 | — |
| Reactant | 3-Cyclohexene-1-carbonitrile | HCID 66013 | — |
| Product | 1,2,3,4,9,9-Hexachloro-1,4,4a,5,6,7,8,8a-octahydro-1,4-methanonaphthalene-6-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04009200 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-42be863f007f449a97e706d96241863c |
| Source note | uspto-grants-1977_02 |