HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 68832696, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 68832620 | HCID 68832620 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68832696 | HCID 68832696 | — |
Reaction Steps
To a solution of 5-acetyl-2-(4-fluorobenzyl)-7-(hydroxymethyl)-2,5-diazabicyclo[4.1.0]heptane-3-one (1.3 g, 4.45 mmol) in 40 mL anhydrous THF under nitrogen, sodium hydride (60% in mineral oil, 231 mg, 5.78 mmol) was added. After stirring for 1 h, benzyl bromide (0.58 ml, 4.89 mmol) in THF (1 mL) was added. The reaction mixture was stirred at room temperature overnight. The reaction was quenched with saturated aqueous ammonium chloride solution. The aqueous layer was extracted with chloroform three times. The combined organic phases were dried over sodium sulfate, filtered and concentrated. The residue was purified by column chromatography on silica gel using hexanes and ethyl acetate as eluents to give the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517532B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-1e04fd4c9ec1490da2a3faeb3a07d95c |
| Source note | uspto-grants-2009_04 |