HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978019Generated: October 27, 2026
N-Methylcyclohexylamine → 4-Chloro-N-cyclohexyl-N-methylbutanamide
https://huagongshe.com/reaction/978019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-N-cyclohexyl-N-methylbutanamide | HCID 13208297 | — |
Reaction Steps
To ethyl acetate (400 ml) is added N-methylcyclohexylamine (26 ml), and to the mixture are added dropwise with stirring 4-chlorobutyryl chloride (25 ml) and triethylamine (33.5 ml) over a period of 20 minutes with keeping the inner temperature at 10° to 20° C. by ice-cooling. The mixture is further stirred at room temperature for one hour. After the reaction, water is added to the reaction mixture. The organic layer is separated and washed with water and aqueious saturated potassium carbonate solution, 10% hydrochloric acid and water in order, and then dried over anhydrous sodium sulfate. After filtering off sodium sulfate, the mother liquor is concentrated and distilled under reduced pressure to give N-methyl-N-cyclohexyl-4-chlorobutyramide (41.5 g), b.p. 133°-136° C./2 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04663323 |
|---|
| Source dataset | uspto-grants-1987_05 |
|---|
| ORD ID | ord-f2e6e344cebd4de4bcd21ac08395917a |
|---|
| Source note | uspto-grants-1987_05 |
|---|