HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 4-Cyclopropylmethoxydibenzo[b,d]furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | 4-Dibenzofuranol | HCID 3015051 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Cyclopropylmethoxydibenzo[b,d]furan | HCID 69282483 | 90% |
Reaction Steps
A solution of Dibenzo[b,d]furan-4-ol (1 g, 5.43 mmol) in DMF (5 ml) was added to a stirred and cooled (0° C.) suspension of 60% sodium hydride (326 mg, 8.12 mmol) in DMF (20 ml). The mixture was stirred at 0° C. for 5 min and cyclopropylmethyl bromide (1.31 g, 10.85 mmol) in DMF (5 ml) was added dropwise over a period of 10 min. The cooling bath was removed and the mixture was stirred for 1 h at room temperature. The reaction mixture was diluted with ice-cold water (100 ml) and extracted with EtOAc (3×50 ml). The combined organic extracts were washed with water (2×100 ml), brine (100 ml) and dried (Na2SO4), to give 1.16 g (90%) of the product as viscous liquid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238725B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-cf811004c58441f58ca20fdad893b1af |
| Source note | uspto-grants-2007_07 |