Reaction of dimethyl 2-methyl- and dimethyl 2-phenyl-4-oxo-4H-chromen-3-yl-phosphonate with amines
✍ Scribed by Budzisz Elż; Pastuszko Slawomir
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 490 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
The reaction of dimethyl 2-methyl-and dimethyl 2-phenyl-4-oxo-4H-chromen-3-yl-phosphonate with various aliphatic and aromatic amines was investigated. A novel class of cyclic phosphonic analogues of ehromone, 1 (2-methoxy-3-[l-(alkylamino)ethylidene or benzylidene]-2,3-dihydro-2,4-dioxo-2~.%benzo[e]--[1,2]oxaphosphinane), was obtained when primary amines were used as nucleophiles. An analogous reaction with aromatic or secondary amines led to the hydrolysis of one methyl ester group in the phosphonic acid residue.
📜 SIMILAR VOLUMES
Single-crystal X-ray study T = 294 K Mean (C-C) = 0.006 A Disorder in solvent or counterion R factor = 0.046 wR factor = 0.133 Data-to-parameter ratio = 12.5 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
In the title compound, C 25 H 23 N 3 O 4 S, the central benzene ring makes dihedral angles of 8. 73 (3), 68.16 (7) and41.67 (7) with the pyrazolone ring, the sulfur-bound benzene ring and the phenyl ring, respectively. The crystal packing is stabilized by a weak non-classical intermolecular C-HÁ Á Á