Tetrahydrofuran → HCID 13092010, compound
Reaction equation
[OH:1][CH:2]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[C:14]([F:17])([F:16])[F:15])[C:3](=[NH:7])[O:4]CC.[O:18]1CCC[CH2:19]1>C1(C)C=CC=CC=1>[F:17][C:14]([F:15])([F:16])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=1[CH:2]1[O:1][C:19](=[O:18])[NH:4][C:3]1=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By the procedure of Method A of Example 12, ethyl 1-hydroxy-1-(2-trifluoromethylphenyl)methanecarboximidate (10 g.) in 500 ml. of tetrahydrofuran was converted to toluene recrystallized 5-(2-trifluoromethylphenyl)oxazolidine-2,4-dione (5.3 g., 54%; m.p. 91°-93° C.; m/e 245).
Workup
- customrecrystallized 5-(2-trifluoromethylphenyl)oxazolidine-2,4-dione (5.3 g., 54%; m.p. 91°-93° C.; m/e 245)
Sources & evidence
- ORD record
- ord-1ec0c2fae2314cc88d198a9f3d5c75e1
- Source dataset
- uspto-grants-1983_01
- Patent number
- US04367234
Reaction notes
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