Hydroxyamine hydrochloride → HCID 18950314, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:19])[C:9](=[CH:15]OCC)[C:10]([CH:12]2[CH2:14][CH2:13]2)=[O:11])=[C:4]([S:20][CH3:21])[C:3]=1[CH2:22][S:23][CH3:24].Cl.[NH2:26]O.C([O-])(=O)C.[Na+]>C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:9]2[CH:15]=[N:26][O:11][C:10]=2[CH:12]2[CH2:14][CH2:13]2)=[O:19])=[C:4]([S:20][CH3:21])[C:3]=1[CH2:22][S:23][CH3:24]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1-[4-chloro-3-(methylsulphenylmethyl)-2-(methylsulphenyl)phenyl]-2-ethoxymethylene-3-cyclopropylpropan-1,3-dione (2.3 g), hydroxylamine hydrochloride (0.52 g) and sodium acetate (0.46 g) in ethanol was stirred at room temperature overnight. The resulting mixture was filtered and the solid collected, washed with water and air dried to yield 4-[4-chloro-2-(methylsulphenyl)-3-(methylsulphenylmethyl)benzoyl]-5-cyclopropylisoxazole (Compound 3, 0.46 g) as a yellow solid, m.p. 79.9°-80.5° C.
Workup
- filtrationThe resulting mixture was filtered
- customthe solid collected
- washwashed with water and air
- customdried
Sources & evidence
- ORD record
- ord-01dca6888c8046d789d189addf76d504
- Source dataset
- uspto-grants-1994_12
- Patent number
- US05374606
Reaction notes
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