HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Diethyl 2-(3'-{[methyl-(1-phenylmethanoyl)-amino]methyl}biphenyl-4-ylmethyl)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diethyl 2-(3'-{[methyl-(1-phenylmethanoyl)amino]methyl}biphenyl-4-ylmethylene)malonate | HCID 22341469 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Diethyl 2-(3'-{[methyl-(1-phenylmethanoyl)-amino]methyl}biphenyl-4-ylmethyl)malonate | HCID 22341493 | — |
Reaction Steps
700 mg (1.5 mmol) of diethyl 2-(3′-{[methyl-(1-phenylmethanoyl)amino]methyl}biphenyl-4-ylmethylene)malonate, 7 ml of THF and 1 ml of methanol are introduced into a three-necked flask under a stream of nitrogen. The reaction medium is degassed, 80 mg of palladium-on-charcoal (5%) are introduced and the mixture is hydrogenated under atmospheric pressure at room temperature for 20 hours. The reaction medium is filtered through Celite and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a mixture of heptane and ethyl acetate (80/20). After evaporation of the solvents, 450 mg (63%) of the desired product are collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06927228B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-d3bc1959691e48688917894e1f76aa21 |
| Source note | uspto-grants-2005_08 |