Reaktionsgleichung
ON=[C:3]([C:8]1[CH:9]=[N:10][S:11][CH:12]=1)[C:4]([O:6]C)=[O:5].C=[O:14].Cl>O>[S:11]1[CH:12]=[C:8]([C:3](=[O:14])[C:4]([OH:6])=[O:5])[CH:9]=[N:10]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of methyl 2-hydroxyimino-2-(isothiazol-4-yl)acetate (anti isomer) (3.41 g.), 36% aqueous solution of formaldehyde (24 ml.), conc. hydrochloric acid (12 ml.) and water (24 ml.) was stirred for 7 hours at 90° to 100° C. The reaction mixture was allowed to stand overnight in a refrigerator to precipitate crystals. The crystals were collected by filtration, washed with a small amount of ice-water and then dried to give 2-(isothiazol-4-yl)glyoxylic acid (2.09 g.). The mother liquor was extracted with ethyl acetate to give the same compound (0.34 g.), mp 145° to 148° C.
Aufarbeitung
- waitto stand overnight in a refrigerator
- customto precipitate crystals
- filtrationThe crystals were collected by filtration
- washwashed with a small amount of ice-water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-abdf94a3650e45b8b1d8155143a07b00
- Quelldatensatz
- uspto-grants-1982_09
- Patentnummer
- US04350693
Verknüpfte Notizen
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