HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Butylaniline | HCID 7694 | — |
| Reactant | 5-(benzyloxy)-4-oxo-4H-pyran-2-carboxylic acid | HCID 6480782 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-one | HCID 67419599 | — |
Reaction Steps
A suspension of 4-butylaniline (0.6 g, 4.1 mmol) and 5-(benzyloxy)-4-oxo-4H-pyran-2-carboxylic acid (1.0 g, 4.1 mmol) in a 1:1 mixture of AcOH:water (4 mL) was heated in a sealed reaction vessel at 120° C. for 72 h. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure, diluted with 10 mL 10% aq. NaOH, and extracted with EtOAc (3×10 mL). The organic fractions were pooled, dried (Na2SO4), and concentrated under reduced pressure to provide 3-(benzyloxy)-1-(4-butylphenyl)pyridin-4(1H)-one, which was used in the subsequent step without further purification. LC/MS (M+H)+ 334.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024032B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-fa4b12df1ed64313b4ac5c9090e3be8c |
| Source note | uspto-grants-2015_05 |