HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Formate → Benzhydryl 4-hydroxy-3-oxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | Benzhydryl 4-bromo-3-oxobutyrate | HCID 15080911 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzhydryl 4-hydroxy-3-oxobutanoate | HCID 24978293 | 47.1% |
Reaction Steps
To a solution of 4-bromo-3-ketobutyric acid diphenylmethyl ester (2b, 11.4 g, 32.8 millimoles) in methanol dried with Molecular Sieves is added sodium formate (3.40 g, 50.0 millimoles), and the mixture is refluxed for 4 hours. The reaction mixture is filtered to remove solid material concentrated under reduced pressure, and extracted with ethyl acetate. The extract is washed with water, dried over magnesium sulfate and evaporated to remove the solvent. The residue is purified by chromatography over Lobar® column B using a mixture of benzene and ethyl acetate (3:1) as eluting solvent to afford the title compound (3b, 4.39 g, 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539148 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-eaa249dda5a74863b234449441bfd8ba |
| Source note | uspto-grants-1985_09 |