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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192257Generated: November 1, 2026

Hydrochloric Acid → 6-Sulfanyl-2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/1192257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-sulfonyl chlorideHCID 5200229—
ReactantTin atomHCID 5352426—
Solvent1,4-DioxaneHCID 31275—
Product6-Sulfanyl-2H-1,4-benzoxazin-3(4H)-oneHCID 1622778916.1%

Reaction Steps

To a solution of 3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-sulfonyl chloride (5.8 g, 20.2 mmol), was added the hydrogen chloride in 1,4-dioxane (30 mL) followed by tin powder (12 g, 10.1 mmol). The resulting mixture was heated under reflux for 2 hours. After this time, the solvent of the reaction mixture was removed under vacuum to give the crude residue. The resulting residue was treated with ethyl acetate and washed with brine and water. The organic layer was separated, dried (Na2SO4) and concentrated. The crude material was purified by silica gel chromatography using a 60:40 mixture of hexane and ethyl acetate as eluent to afford the title product as a white solid (0.59 g, 16% yield). 1H NMR (400 MHz, d6-DMSO) δ: 10.82 (1H, s), 6.86 (2H, m), 6.81 (1H, m), 5.40 (1H, s), 4.53 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680139B2
Source datasetuspto-grants-2014_03
ORD IDord-f92917e49b9b4f7392d5cfea292906fd
Source noteuspto-grants-2014_03