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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224061Generated: November 2, 2026

Hydrochloric Acid → HCID 58641530, compound

https://huagongshe.com/reaction/2224061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
ReactantHCID 22312860HCID 22312860—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58641530HCID 5864153083%

Reaction Steps

A suspension of 6-benzenesulfonyl-4H-benzo[1,4]oxazin-3-one (1.42 g g., 4.9 mmol) in 10 ml anhydrous THF was brought to reflux, and borane-dimethyl sulfide complex (2.45 mL, 10 M in THF, 24.5 mmol) was added dropwise via syringe. The solution was refluxed for 3 hours, and the solution was cooled to room temperature and ethanolic HCl (3 mL, 2 N) was added dropwise. The resulting solution was refluxed for 1 hour and then cooled to room temperature. The reaction mixture was poured into 50 mL water, the resulting solution made basic with potassium carbonate and extracted three times with 25 mL Et2O. The organic fractions were washed with 50 mL brine, dried over Na2SO4 and concentrated in vacuo. The resulting residue was purified by flash chromatography (30 to 50% EtOAc in hexanes) to give 1.12 g of 6-benzenesulfonyl-3,4-dihydro-2H-benzo[1,4]oxazine (83%) as a yellow solid. MS: 276 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378415B2
Source datasetuspto-grants-2008_05
ORD IDord-f8a78b359cb7408c821ac485fa29f688
Source noteuspto-grants-2008_05