HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-Butyl-1-phenylpyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 3-Hydroxymethylheptanoic acid phenylamide | HCID 69312033 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Butyl-1-phenylpyrrolidin-2-one | HCID 17952438 | 72% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 3-hydroxymethylheptanoic acid phenylamide (0.61 g, 2.6 mmol) in THF (30 mL) under argon was added triphenylphosphine (1.36 g, 5.2 mmol). The solution was cooled to 0° C. and diethyl azodicarboxylate (0.61 mL, 3.9 mmol) was added dropwise. The reaction mixture was warmed up to rt and stirred overnight. The reaction was quenched with saturated aqueous NaHCO3 (50 mL) and extracted with dichloromethane (3×50 mL). The combined extractions were dried (Na2SO4), filtered and concentrated. The residue was purified by flash column chromatography (silica gel, ethyl acetate/hexanes 1:2) to afford 4-butyl-1-phenylpyrrolidin-2-one as a white solid (0.4 g, 72%). MS(ES) m/e 218 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07456211B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-8d43c8feb4254c3b9264d070f66bb0fa |
| Source note | uspto-grants-2008_11 |