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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841852Generated: October 26, 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/reaction/841852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazineHCID 22617346—
SolventDichloromethaneHCID 6344—
SolventMethyl, chloro-HCID 5378701—
Product3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazine-4,4-dioxideHCID 22617360103.3%

Reaction Conditions

Temperature30 °C

Reaction Steps

3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazine (12g, 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 (34g, 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., 14.3g, Found: C 33.27, H 2.33, N 5.55; C7H6ClNO3S2 requires C 33.40, H 2.39, N 5.57).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372297B1
Source datasetuspto-grants-2002_04
ORD IDord-8164493e8a174649aa9bc3e6d25bac6f
Source noteuspto-grants-2002_04