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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,2-trimethylaziridine-1-carboxamideHCID 11007919—
Reactant1,2-Difluoro-3-propoxybenzeneHCID 14495775—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178447976HCID 178447976—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 178458364HCID 178458364—

Reaction Conditions

Temperature-40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236620
Source datasetuspto-grants-1993_08
ORD IDord-4ce1ec3aecaf4d5aac8a5addbb4e79b5
Source noteuspto-grants-1993_08