HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Tetrabenzylpentaerythritol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Pentaerythritol | HCID 8285 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tetrabenzylpentaerythritol | HCID 12082528 | 38% |
Reaction Steps
Sodium hydride (440 mg, 11.01 mmol) and benzyl bromide (1.3 mL, 11.01 mmol) were added to 20 mL of a solution of pentaerythritol (500 mg, 3.67 mmol) in DMF, and the mixture was stirred at room temperature for 14 hours. Aqueous saturated ammonium chloride was added to the mixture, followed by extraction with ethyl acetate. The extract was washed with saturated saline and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1) to obtain 3-benzyloxy-2,2-bis(benzyloxymethyl)propan-1-ol (560 mg, 38%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820693B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-3fbdb400f3c4428d914202e1fbe3853f |
| Source note | uspto-grants-2010_10 |