HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-(2-Benzyloxy-ethyl)-3-bromo-benzo[b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 821949 | HCID 821949 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Benzyloxy-ethyl)-3-bromo-benzo[b]thiophene | HCID 58591558 | 87.6% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a cooled solution (0° C.) of 2-(3-bromo-benzo[b]thiophen-2-yl)-ethanol (7.7 g, 29.9 mmol) in DMF (40 mL), NaH (1.44 g, 59.8 mmol, 95%) was added and the mixture was stirred for 20 min at 0° C. Subsequently benzylbromide (5.3 mL, 45 mmol) was added and the mixture was stirred overnight while the temperature gradually reached room temperature. After quenching with MeOH, the mixture was concentrated in vacuo, dissolved in EtOAc, washed with sat NaHCO3, brine, dried (Na2SO4) and concentrated in vacuo. Purification by silica gel column chromatography (eluent: EtOAc/Hexanes=1/1) afforded 9.1 g of 2-(2-benzyloxy-ethyl)-3-bromo-benzo[b]thiophene (87% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393865B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-c671ffe1551b4822ac34247c47b82dc2 |
| Source note | uspto-grants-2008_07 |