HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-Cyclopentyloxy-2-methylbenzo[b]furan-4-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Hydroxy-2-methylbenzo[b]furan-4-carbaldehyde | HCID 82410992 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Cyclopentyloxy-2-methylbenzo[b]furan-4-carboxaldehyde | HCID 44247882 | 101.9% |
Reaction Steps
To a well stirred suspension of 7-Hydroxy-2-methylbenzo[b]furan-4-carbaldehyde (39.0 g, 0.221 moles) in DMF (200 mL) was added powdered potassium carbonate (76.0 g, 0.555 moles) and cyclopentyl bromide (43.0 g, 0.287 moles) and stirred at 70-75° C. for 4-5 hrs. The reaction mixture was then cooled to room temperature and water (1.5 L) was added to it. The organic material separated was extracted with ethyl acetate (3×100 ml). The combined organic layers were washed with water ((2×500 mL) and dried over anhydrous sodium sulfate. Removal of solvent under vacuo gave product (55.0 g) as light brown viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129401B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-8c78252483404a70b1bf8d53ef0a93f6 |
| Source note | uspto-grants-2012_03 |