Hydrochloric Acid → 2-[2-(4-Fluorophenyl)ethyl]-5,6-dihydro-4,4,6-trimethyl-4H-1,3-oxazine
Reaction equation
[CH3:1][C:2]1[O:3][CH:4]([CH3:10])[CH2:5][C:6]([CH3:9])([CH3:8])[N:7]=1.C([Li])CCC.[F:16][C:17]1[CH:24]=[CH:23][C:20]([CH2:21]Cl)=[CH:19][CH:18]=1.Cl>O1CCCC1.CCCCCC.O>[CH3:8][C:6]1([CH3:9])[CH2:5][CH:4]([CH3:10])[O:3][C:2]([CH2:1][CH2:21][C:20]2[CH:23]=[CH:24][C:17]([F:16])=[CH:18][CH:19]=2)=[N:7]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
5,6-Dihydro-2,4,4,6-tetramethyl-4H-1,3-oxazine (10.98 g) in anhydrous tetrahydrofuran (80 ml) was cooled to -70° under nitrogen. n-Butyllithium in hexane (44 ml) was added dropwise to the stirred solution over approximately 1 hr and the mixture was stirred for a further hour. 4-Fluorobenzyl chloride (12.38 g) in anhydrous tetrahydrofuran (20 ml) was added to the mixture over 30 min and the stirred reaction mixture was allowed to warm to room temperature overnight. The mixture was poured into iced water (100 ml) and adjusted to pH 2-3 with 9 M hydrochloric acid. The solution was extracted with pentane (3×75 ml), then adjusted to pH 14 with 10 M sodium hydroxide, and the resulting oil was extracted with ether (3×75 ml). The solvent was evaporated to give crude 5,6-dihydro-4,4,6-trimethyl-2-[2-(4-fluorophenyl)ethyl]-4H-1,3-oxazine (13.87 g).
Workup
- customthe stirred reaction mixture
- extractionThe solution was extracted with pentane (3×75 ml)
- extractionthe resulting oil was extracted with ether (3×75 ml)
- customThe solvent was evaporated
Sources & evidence
- ORD record
- ord-46aee925f09d4a46bfad6c7d7d38cd98
- Source dataset
- uspto-grants-1979_07
- Patent number
- US04160036
Reaction notes
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