Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hexyne | HCID 12732 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 22494906 | HCID 22494906 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 13547115 | HCID 13547115 | — |
Reaction Steps
A solution of 22 g of hexyne in 300 ml of THF was placed in a flask, and cooled to -50° C. Then, 170 ml of a 1.55M n-hexane solution of n-butyllithium was dropped thereto. The resulting mixture was stirred at -50° C. for 15 minutes, and then a solution of 50 g of (S) 1-ethoxyethyl-N,N-dimethyllactamide as obtained in Example 1 (2) in 150 ml of THF was dropped thereto. The resulting mixture was stirred at the same temperature as above for two hours, and then an aqueous solution of 28.3 g of ammonium chloride in 200 ml of water was dropped to terminate the reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05164112 |
|---|
| Source dataset | uspto-grants-1992_11 |
|---|
| ORD ID | ord-b9465580811e4feb8cf5d726ac5575ea |
|---|
| Source note | uspto-grants-1992_11 |
|---|