HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 19432448, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 19432446 | HCID 19432446 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19432448 | HCID 19432448 | 82.6% |
Reaction Steps
To a solution of 3-bromo-7-hydroxymethyldibenzofuran (2.74 g, 9.9 mmol) and t-butyldimethylsilyl chloride (1.93 g, 12.8 mmol) in THF (60 ml) was added triethylamine (1.95 ml, 13.8 mmol) followed by 4-dimethylaminopyridine (DMAP) (120.7 mg, 0.99 mmol). After stirring at room temperature for 20 hours, the solution was poured into ethyl ether (180 ml) and washed successively with saturated NH4Cl, saturated NaHCO3, H2O and brine. Drying (MgSO4) and evaporation gave a brown solid which was purified by flash chromatoraphy through 100 g silica gel (10% CH2Cl2 hexane) to yield 3.2 g (82%) of the title compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534507 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-529f9642db9f42c9aabc009505a545d7 |
| Source note | uspto-grants-1996_07 |