HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254491Generated: October 31, 2026
N,N,2-trimethylaziridine-1-carboxamide → HCID 178458364, compound
https://huagongshe.com/reaction/2254491
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,2-trimethylaziridine-1-carboxamide | HCID 11007919 | — |
| Reactant | 1,2-Difluoro-3-propoxybenzene | HCID 14495775 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178447976 | HCID 178447976 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178458364 | HCID 178458364 | — |
Reaction Steps
65 ml of a solution of 0.1 mol of n-butyllithium in hexane is added at -100° C. to a mixture of 0.1 mol of 4- propoxy-2,3-difluorobenzene, 0.09 mol of potassium tert.butylate and 250 ml of tetrahydrofuran. After stirring for 10 minutes a mixture of 0.1 mole of trans-4-(trans-4-propylcyclohexylethyl)-cyclohexylethyl iodide, 0.1 mol of N,N-dimethylpropyleneurea and 100 ml of tetrahydrofuran is added to the mixture. Stirring for 1 hour at -85° C., warming up to -40° C. and working up in the customary manner gives trans-4-(2-(4-propoxy-2,3-difluorophenyl)-ethyl)-1-(2-(trans-4-propylcyclohexyl)ethyl)-cyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05236620 |
|---|
| Source dataset | uspto-grants-1993_08 |
|---|
| ORD ID | ord-4ce1ec3aecaf4d5aac8a5addbb4e79b5 |
|---|
| Source note | uspto-grants-1993_08 |
|---|