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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461756Generated: October 27, 2026

Norborna-diene → Binor-S

https://huagongshe.com/reaction/461756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorborna-dieneHCID 18006658—
SolventDichloromethaneHCID 6344—
ProductBinor-SHCID 101172629—

Reaction Steps

Norbornadiene (bicyclo[2.2.1]hepta-2,5-diene) was dimerized with the catalyst system CoBr2 -(triphenylphosphine)2 -boron trifluoride etherate. The structure of the diene is as follows: ##STR3## Afterwards methylene chloride was used to dissolve the organic phase of the reaction mixture and to separate the latter from the inorganic phase of catalyst components. Then the methylene chloride solution was washed with potassium carbonate to neutralize any free halogen acid and dried with the use of a drying agent such as anhydrous sodium sulfate. Upon cooling the treated methylene chloride solution Binor-S crystallized. The crystals were filtered from the liquid and then vacuum distilled to give solid Binor-S which had a grayish tinge. The foregoing procedure has been described in the literature. This procedure yields a Binor-S containing a trace amount of indigenous halide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064180
Source datasetuspto-grants-1977_12
ORD IDord-33b65dd3b70e4838a15db2e9667867c4
Source noteuspto-grants-1977_12