Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulphonyl cyanide | HCID 87946 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 19380596 | HCID 19380596 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 15218978 | HCID 15218978 | — |
Reaction Steps
A mixture of 44 mmol of 1B and 80 ml of THF is added dropwise at -78° C. to a solution of 48 mmol of lithium diisopropylamide in hexane. The mixture is stirred at -50° C. for 2 hours and then re-cooled to -78° C., and a mixture of 48 mmol of p-toluenesulphonyl cyanide in 20 ml of THF is slowly added dropwise. After warming to room temperature and conventional work-up, the pure product is obtained by recrystallization from ethanol. C 85 N (75) I, Δε=71.3, Δn=0.232 (extrapolated from ZLI-4792)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05454975 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-defbbbb8bc5a4d2994bd0f6b8eb4d3f2 |
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| Source note | uspto-grants-1995_10 |
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