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HRID 1955950Erstellt: 23. Oktober 2026

Sulfuric acid magnesium salt (1:1) → 3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazine-4,4-dioxide

https://huagongshe.com/de/reaction/1955950

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazineHCID 22617346—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelMethyl, chloro-HCID 5378701—
Produkt3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazine-4,4-dioxideHCID 22617360103,3%

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazine (12 g, 0.055 mol) prepared in Example 1, in methylene chlorine (50 ml) and anhydrous magnesium sulphate (10 g) in suspension, was stirred while m-chloroperoxybenzoic acid (34 g, 50-60% material) in methylene chloride (250 ml), was added dropwise, to prepare a reaction mixture. The reaction mixture was allowed to warm to 30° C. and after the dropwise addition was externally heated to 35° C. for 10 hours by which time a negative starch/Kl test was obtained. Unwanted m-chlorobenzoic acid was then removed from the reaction mixture by extraction with aqueous sodium bicarbonate. The remaining reaction mixture was washed with water, dried (MgSO4) and evaporated to dryness. The resultant residue was chromatographed on 500 g silica gel eluting with methylene chloride, to produce 3-(5-chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazine-4,4-dioxide (mp 113°-114° C., 14.3 g, Found: C 33.27, H 2.33, N 5.55; C7H6ClNO3S2 requires C 33.40, H 2.39, N 5.57).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05777110
Quelldatensatzuspto-grants-1998_07
ORD IDord-d7aacc947e924e50a699a250de1c330b
Quellennotizuspto-grants-1998_07