HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-iso-butylbenzoylformate → 4-hydroxy-5-(4-isobutylphenyl)-3-phenylmethoxy-5-(1-propyl)-2(5H)-furanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-iso-butylbenzoylformate | HCID 12585534 | — |
| Reactant | 3,4-dihydroxy-5-methyl-5-phenyl-2(5H)-furanone | HCID 54725499 | — |
| Reactant | HCID 178455851 | HCID 178455851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-hydroxy-5-(4-isobutylphenyl)-3-phenylmethoxy-5-(1-propyl)-2(5H)-furanone | HCID 70247352 | — |
Reaction Steps
A total of 5.2 mL (10.4 mmol) of 2.0 M 1-propylmagnesium bromide was added to a solution of 2.3 g (10 mmol) of ethyl 4-isobutylbenzoylformate in THF in an analogous manner as described for the synthesis of 3,4-dihydroxy-5-methyl-5-phenyl-2(5H)-furanone to provide 4-hydroxy-5-(4-isobutylphenyl)-3-phenylmethoxy-5-(1-propyl)-2(5H)-furanone as an oil, which was purified over SiO2 using acetone/hexanes (1/4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06005000 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-133ea2964e2e4d50adf72bd92401e5db |
| Source note | uspto-grants-1999_12 |