4-Benzylphenol → (4-Benzylphenoxy)acetonitrile

18.4 g of 4-benzylphenol was dissolved in 100 ml of anhydrous tetrahydrofuran and 4.0 g of sodium hydride (60 % oil dispersion) was gradually added to the solution with ice cooling :n nitrogen stream. The solution was stirred for 1 hour at room temperature and 12.0 g of bromoacetonitrile was added thereto under ice cooling, followed by refluxing with heating for 3 hours. After being left for cooling, the reaction mixture was concentrated under reduced pressure and to the residue was added 100 ml of water, followed by extracting twice with 100 ml of chloroform. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain an oily residue. The residue was chromatographed on a silica gel column (eluting solvent hexane : acetone=3 : 1 (v/v)) to obtain 19.1 g of (4-benzylphenoxy)acetonitrile.

1. temperatureby refluxing
2. temperaturewith heating for 3 hours
3. waitAfter being left
4. temperaturefor cooling
5. concentrationthe reaction mixture was concentrated under reduced pressure and to the residue
6. additionwas added 100 ml of water
7. extractionby extracting twice with 100 ml of chloroform
8. washThe extract was washed with water
9. dry with materialdried over anhydrous magnesium sulfate
10. concentrationconcentrated under reduced pressure
11. customto obtain an oily residue
12. customThe residue was chromatographed on a silica gel column (eluting solvent hexane : acetone=3 : 1 (v/v))

ORD record

ord-6b2e93c9b7524f0fa6c2bab1eb6856a6

Source dataset

uspto-grants-1993_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05236924