HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethynylcyclohexylamine → HCID 12939913, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethynylcyclohexylamine | HCID 121691 | — |
| Reactant | 1-[2-Cyano-4-(isobutyroyl-amino)-phenoxy]-2,3-epoxy-propane | HCID 23318127 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12939913 | HCID 12939913 | — |
Reaction Steps
7.8 gm (0.03 mol) of 1-[2-cyano-4-(isobutyroyl-amino)-phenoxy]-2,3-epoxy-propane were dissolved in 80 ml of ethanol, and after addition of 7.5 gm (0.06 mol) of 1-ethinyl-cyclohexyl-amine the mixture was refluxed for one hour. The solvent was then distilled off, and the residue was acidified with dilute HCl. After extraction with ethyl acetate the aqueous phase was made alkaline by addition of NaOH, whereby basic components precipitated in oily form. They were taken up in ethyl acetate, the organic phase was washed with water, dried over MgSO4, evaporated and the solid residue was recrystallized twice from acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04344964 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-1bc5ffdd6ad2418a94a352058c4ea0a0 |
| Source note | uspto-grants-1982_08 |