HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl trifluoroacetate → Acetamide, N-(2-aminocyclohexyl)-2,2,2-trifluoro-, cis-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 1,2-Diaminocyclohexane, cis- | HCID 342917 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Acetamide, N-(2-aminocyclohexyl)-2,2,2-trifluoro-, cis- | HCID 11042018 | — |
Reaction Steps
cis-Cyclohexane-1,2-diamine (5.00 g, 43.9 mmol, 1.00 eq) was charged to a 250 ml, three-neck round bottom flask equipped with an overhead stirrer and a thermocouple. Ethanol (50 mL) was added and the solution was cooled to <0° C. using an ice-brine bath. A solution of ethyl trifluoroacetate (6.23 g, 1.00 eq) in EtOH (25 mL) was added via a syringe pump over a one hour period. Once the addition was complete, the cooling bath was removed and the solution was slowly warmed to RT and stirred for 3.5 hours to afford the title compound in EtOH. Half (41 mL, about 21.9 mmol) of the total solution (about 82 mL) was carried into the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181255B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-62478a3501d04b30ba976b92bb573c84 |
| Source note | uspto-grants-2015_11 |