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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841851Generated: October 27, 2026

1,2-Dibromoethane → 3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazine

https://huagongshe.com/reaction/841851

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 53986717HCID 53986717—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-(5-Chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazineHCID 22617346—

Reaction Conditions

Temperature5 °C

Reaction Steps

Methyl 5-chloro-2-thiophenecarbodithioate (61.4g, 0.29 mol) was suspended in methanol (400 ml) with finely powdered hydroxylamine hydrochloride (25g). With stirring, triethylamine (50 ml) in methanol (50 ml) was added dropwise to the suspension, to produce a reaction mixture. During this addition, the reaction mixture was cooled to 5° C. Stirring of the reaction mixture was continued until an orange (from red) color developed in the reaction mixture. Additional triethylamine (100 ml) was then added at once, followed by 1,2-dibromoethane (20 ml). The resultant reaction mixture was then stirred overnight at ambient temperature. The reaction mixture was then refluxed with removal of solvent until a precipitate appeared. The reaction mixture was then cooled and water was added. The reaction mixture was then filtered and the solid collected on the filter was recrystallized from ethanol to produce 3-(5-chloro-2-thienyl)-5,6-dihydro-1,4,2-oxathiazine (mp 74-77° C., 21.4g. Found C 38.5, H 2.94, N 6.45, C7H6CINOS2 requires C 38.27, H 2.73, N 6.38)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372297B1
Source datasetuspto-grants-2002_04
ORD IDord-44b801f4036446b6809043419931eea1
Source noteuspto-grants-2002_04