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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939612Generated: October 31, 2026

1,2-Dibromoethane → HCID 22104147, compound

https://huagongshe.com/reaction/1939612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantBenzoic acid, 2-[(phenylmethyl)thio]-, methyl esterHCID 775668—
SolventMethanolHCID 887—
ProductHCID 22104147HCID 2210414721.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

160 g (2.86 mol) of potassium hydroxide in 700 ml of methanol are added dropwise, at room temperature, to a mixture of 98.7 g (1.42 mol) of hydroxylamine hydrochloride and 700 ml of methanol. Subsequently, 184 g (0.712 mol) of methyl 2-(benzylthio)benzoate are added in portions at room temperature. The mixture is stirred at 40° C. overnight. 98.1 g (0.712 mol) of potassium carbonate are then added, 601 g (3.20 mol) of 1,2-dibromoethane are added dropwise, and the mixture is left stirring at 60° C. overnight. Subsequently, the solvent is distilled off under reduced pressure. The residue is partitioned between methylene chloride and water. The organic phase is dried and the solvent is distilled off under reduced pressure. The residue is stirred up with absolute ethyl alcohol. The solid is filtered off with suction and dried under high vacuum. 43.1 g (21% of theory) of 1-benzylthio-2-(5,6-dihydro-[1,4,2]-dioxazin-3-yl)benzene are obtained as a pale yellow solid. Melting point: 73°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696257
Source datasetuspto-grants-1997_12
ORD IDord-100118ea4d22424ebc442eb03511fc14
Source noteuspto-grants-1997_12