HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4-Formylbenzoate → methyl (E)-4-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4-Formylbenzoate | HCID 15294 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl Dimethylphosphonoacetate | HCID 4564495 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl (E)-4-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)benzoate | HCID 42640359 | 118.3% |
Reaction Steps
To a solution of tert-butyl P,P-dimethylphosphonoacetate (Fluka, 1.43 g, 6.4 mmol) in THF (40 mL) was added NaH (Alderich, 60%, 536 mg, 13.4 mmol) portionwise at rt over 30 min. Methyl 4-formylbenzoate (Alderich, 1.0 g, 6.09 mmol) was then added and the reaction mixture was stirred at rt for 4 hrs. The reaction was quenched with water and extracted with EtOAc. The organic layer was separated, and dried over Na2SO4. The mixture was then concentrated to give the crude 4-((E)-2-tert-butoxycarbonyl-vinyl)-benzoic acid methyl ester (1.89 g, 118%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017607B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-09c271f329b44f38b9aa45aa3dea52b2 |
| Source note | uspto-grants-2011_09 |