Tetrahydrofuran → HCID 13092009, compound
Reaction equation
Cl.[OH:2][CH:3]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH3:15])[C:4](=[NH:8])[O:5]CC.[O:16]1CCC[CH2:17]1>C1(C)C=CC=CC=1>[CH3:15][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[CH:3]1[O:2][C:17](=[O:16])[NH:5][C:4]1=[O:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By the procedure of Example 3, ethyl 1-hydroxy-1-(2-methylphenyl)methanecarboximidate hydrochloride (14.4 g.) in 500 ml. of tetrahydrofuran was converted to toluene recrystallized 5-(2-methylphenyl)oxazolidine-2,4-dione (9.1 g., 77%, m.p. 111°-113° C., m/e 191).
Workup
- customrecrystallized 5-(2-methylphenyl)oxazolidine-2,4-dione (9.1 g., 77%, m.p. 111°-113° C., m/e 191)
Sources & evidence
- ORD record
- ord-c1a6009eca3d4b5b8c0f5902e05c1b98
- Source dataset
- uspto-grants-1983_01
- Patent number
- US04367234
Reaction notes
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