The cyclodimerisation of 3-methyl-2-butenenitrile
β Scribed by H Tucker; G Golding; SR Purvis
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 168 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
3-Methyl-2-butenenitrile (1) cyclodimerised on treatment with lithium diisopropylamide in dimethoxyethane at temperatures between -78Β°C and 0Β°C to 3-amino-4-cyano-1,5,5trimethyl-1,3-cyclohexadiene (2) the structure of which was established by acid hydrolysis to the known 4-cyano-1,5,5-trimethyl-1-cyclohexene-3-one (3).
π SIMILAR VOLUMES
The catalytic isomerization reaction of 2-methyl-3-butenenitrile (2M3BN) into 3-pentenenitrile (3PN) has been performed in the presence of Ni(0) and phosphine complexes and in biphasic ionic liquid/organic solvent. Several neutral and ionic phosphines and ionic liquids have been tested, the best res
The catalytic isomerization of 2-methyl-3-butenenitrile (2M3BN) was performed in the presence of Ni(0) with N-heterocyclic carbene (NHC) ligands. On using bulky aromatic substituents on the NHC nitrogen atoms, the isomerization reaction proceeded at room temperature within 15 min: a total conversion