HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N,N',N'-Tetramethylethylenediamine → HCID 178447957, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178447956 | HCID 178447956 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178447957 | HCID 178447957 | — |
Reaction Steps
A solution of 0.1 m of 1-(trans-4-n-propylcyclo-hexyl)-2-(3,3′, 5′-trifluorobiphenylyl)ethane and 0.1 m of TMEDA in 300 ml of THF is treated dropwise at about -65° with 0.1 m of n-BuLi (1.5 M in hexane). The mixture is stirred at this temperature for a further 30 minutes, and 0.2 m of N-chlorosuccinimide in 70 ml of THF is then slowly added. When the addition is complete, the mixture is allowed to warm to −20° and is hydrolyzed using H2O. The product is dissolved completely by adding diethyl ether. Extractive work-up and purification by chromatography and crystallization give l-(trans-4-n-propylcyclohexyl)-2-(4′-chloro-3,3′, 5′-trifluorobiphenylyl)ethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06326066B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-6ca0bc0beb764b12ad6eb69bf317b47c |
| Source note | uspto-grants-2001_12 |