HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Cyclohexylcyclohexanemethanamine → N,N-Dicyclohexylmethyl-N',N'-dibenzyl-2-butene-1,4-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Cyclohexylcyclohexanemethanamine | HCID 10774245 | — |
| Reactant | 1-Acetoxy-4-dibenzylamino-2-butene | HCID 53789779 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-Dicyclohexylmethyl-N',N'-dibenzyl-2-butene-1,4-diamine | HCID 57036974 | — |
Reaction Steps
A solution of 1-acetoxy-4-dibenzylamino-2-butene (10.1 g, 33 mmol) and dicyclohexylmethylamine (6.8 g, 32 mmol) in 50 ml of THF is treated with tetrakis(triphenylphosphine)palladium (0) (1.0 g, 0.9 mmol) and stirred at room temperature overnight. The reaction mixture is concentrated in vacuo to a solid which is redissolved in 100 ml of THF and treated with 25 ml of 20% aqueous sodium hydroxide. The mixture is stirred for one hour, concentrated and extracted with diethyl ether. The ether extracts are dried and concentrated to give a solid which is then purified by crystallization from isopropanol. The title compound is obtained in a yield of 9.7 g (65%) as a white solid melting at 61°-62° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05283367 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-dad4d83fcf234f899bb21acf4fb32fd9 |
| Source note | uspto-grants-1994_02 |