Chloroacetonitrile → 5-Benzyl-2-(chloromethyl)-1,3-oxazole
Reaction equation
[N+:1](=[CH:3][C:4](=[O:12])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[N-].B(F)(F)F.CCOCC.[Cl:22][CH2:23][C:24]#N>ClCCl>[Cl:22][CH2:23][C:24]1[O:12][C:4]([CH2:5][C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)=[CH:3][N:1]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1-Diazo-3-phenyl-2-propanone (0.8 g, 5 mmol) in dichloromethane (5 ml) was added to a mixture of boron trifluoride diethyl etherate (1.2 ml, 10 mmol), chloroacetonitrile (6.4 ml, 100 mmol) and dichloromethane (5 ml) at 20° C. After 0.5 h at 20° C. the solution was washed with cold aqueous 20% sodium hydroxide, dried (MgSO4), and evaporated under reduced pressure to give an oil which was purified by chromatography (10 g silica, dichloromethane) to give 2-chloromethyl-5-benzyl oxazole as a yellow oil (0.64 g, 62%); δH (CDCl3) 7.2 (5H, S, aryl), 6.7 (1H, S, het-H), 4.5 (2H, S, CH2Cl), 4.2 (2H, S, CH2Ar), 2-Chloromethyl-5-benzyloxazole (0.6 g, 3 mmol) and triethyl phosphite (0.7 ml, 4.5 mmol) were heated together for 1 h at 160° C. and then cooled. Direct chromatography (10 g silica, 0 to 5% methanol in dichloromethane) then gave diethyl 5-benzyl-2-oxazolylmethyl phosphonate as a light brown oil (0.65 g, 70%); δH (CDCl3) 7.2 (5H, S, aryl), 6.7 (1H, S, het-H), 4.1 (4H, m, OCH2), 3.9 (2H, S, CH2Ar), 3.3 (2H, d, CH2P), 1.3 (6H, t, Me).
Workup
- washAfter 0.5 h at 20° C. the solution was washed with cold aqueous 20% sodium hydroxide
- dry with materialdried (MgSO4)
- customevaporated under reduced pressure
- customto give an oil which
- customwas purified by chromatography (10 g silica, dichloromethane)
Sources & evidence
- ORD record
- ord-83dd91b629c543a498c0c34f2b345408
- Source dataset
- uspto-grants-1989_03
- Patent number
- US04812470
Reaction notes
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