HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Dibenzyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Product | Dibenzyl ether | HCID 7657 | — |
Reaction Steps
To a solution of the above alcohol (430 mg, 3.0 mmol) in DMF (10 mL) was added NaH (144 mg of a 60% dispersion in mineral oil, 3.60 mmol) and the mixture was then cooled in an ice bath. Benzyl bromide (437 uL, 3.60 mmol) was then added and the mixture was stirred at room temperature for 3 h. After normal aqueous work-up and short column chromatographic purification, 600 mg of desired benzyl ether was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335657B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-5fcf3e72308241e3b26bd86094ceeeda |
| Source note | uspto-grants-2008_02 |