HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,4-Bis-benzyloxy-5-isopropenyl-benzoic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Benzyl-2,4-bis-benzyloxy-5-bromobenzoate | HCID 46915635 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 2,4-Bis-benzyloxy-5-isopropenyl-benzoic acid benzyl ester | HCID 59263118 | — |
Reaction Steps
To a mixture of 2,4-bis-benzyloxy-5-bromo-benzoic acid benzyl ester (42.9 g, 85.7 mmol), potassium isopropenyl trifluoroborate (14.0 g, 95.2 mmol) and caesium carbonate (83.8 g, 257.1 mmol) in THF (800 mL) was added Pd(PPh3)4 (2.0 g) followed by water (150 mL). The mixture was heated at reflux for 72 h then allowed to cool to ambient. The mixture was reduced in vacuo to remove THF and then partitioned between water (500 mL) and EtOAc (300 mL). The organic portion was washed with brine, dried (MgSO4), filtered and reduced in vacuo to give the title compound (40.9 g) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530469B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-82879779724343929091e26b51fca302 |
| Source note | uspto-grants-2013_09 |