HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethanolamine → N-Cyclohexyl-4,4-dimethyl-3-oxopentanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethanolamine | HCID 7618 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Ethyl pivaloylacetate | HCID 86950 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-Cyclohexyl-4,4-dimethyl-3-oxopentanamide | HCID 13738452 | — |
Reaction Steps
Ethylpivaloylacetate (172 g.), cyclohexylamine (99 g.), triethanolamine (1 g.) and toluene (200 ml.) are mixed in a distillation flask and heated at reflux under a 6 in. Vigreux distillation column. When the head temperature stabilized at 82° C. distillation was begun at a take off to reflux ratio of 1 to 10. Distillation was continued until a head temperature of 110° C. is obtained. The remainder of the solvent is removed in a vacuum and residue is crystallized by trituation with hexane. A yield of 201 g. of product melting at 69°-70° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03993637 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-2fa57a9388fe408f88b73c7e6cd0cb96 |
| Source note | uspto-grants-1976_11 |