Dimethylformamide → Dibenzyl ether
Reaction equation
[H-].[Na+].[CH2:3](Br)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.CN([CH:14]=[O:15])C>>[CH2:3]([O:15][CH2:14][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Participants
4
Procedure
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.
Workup
- temperaturewas then cooled in an ice bath
- customAfter normal aqueous work-up and short column chromatographic purification
Sources & evidence
- ORD record
- ord-2646942418ce43359f515379ea575146
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07078419B2
Reaction notes
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