HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → trans-N-[2-(N,N-dimethylamino)cyclohexyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (1R,2R)-N1,N1-Dimethylcyclohexane-1,2-diamine | HCID 11275066 | — |
| Product | trans-N-[2-(N,N-dimethylamino)cyclohexyl]acetamide | HCID 11735567 | — |
Reaction Steps
This amide was prepared by general procedure A from trans-2-(dimethylamino)cyclohexylamine and acetyl chloride. In the work up the aqueous layer was salted out with solid K2CO3, and extracted well with ether. The resulting oil was crystallized from ether-petroleum ether (30°-60°) to give colorless rods of the sub-titled amide, 79% yield, m.p. 86°-87.5° raised to 88°-89° on recrystallization. ir NH 3280, 3080; N-alkyl 2770; C=O 1660, 1640; amide II 1565. nmr in CDCl3 and 100 MHz was in accord. Mass spectrum M+ 184.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04148914 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-2a2510b7c17045cab93fdfe78cb15e3b |
| Source note | uspto-grants-1979_04 |