Sulfuric Acid → Ethyl 3-(4-methylphenyl)-3-oxopropanoate
Reaction equation
[CH2:1]([O:3][C:4](=[O:15])[CH2:5][C:6](=[O:14])[C:7]1[CH:12]=[CH:11][C:10](Cl)=[CH:9][CH:8]=1)[CH3:2].[CH3:16]NC(=N)S.OS(O)(=O)=O.NC1OC(C2C=CC(SC)=CC=2)=CC(=O)N=1>>[CH2:1]([O:3][C:4](=[O:15])[CH2:5][C:6](=[O:14])[C:7]1[CH:12]=[CH:11][C:10]([CH3:16])=[CH:9][CH:8]=1)[CH3:2]Participants
5
Procedure
The title compound was prepared from ethyl(4-chloro)benzoylacetate (5.0 g, 22 mmol) (obtained in preparation 2) and methylthiopseudourea.H2SO4 (3.31 g, 12 mmol) by following the procedure described in preparation 4, (0.573 g, 11.6%). MS m/z: 223 (M+). Preparation 6 Synthesis of 2-amino-6-(4-methylsulfanyl-phenyl)-1,3-oxazin-4-one
Workup
- customdescribed in preparation 4, (0.573 g, 11.6%)
Sources & evidence
- ORD record
- ord-78979f26236a4b67aa5edcd1ca3d81bb
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07101873B2
Reaction notes
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