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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224085Generated: October 27, 2026

Hydrochloric Acid → 7-benzenesulfonyl-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazine

https://huagongshe.com/reaction/2224085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
Reactant7-benzenesulfonyl-2,2-dimethyl-4H-benzo[1,4]oxazin-3-oneHCID 58641533—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product7-benzenesulfonyl-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazineHCID 5864153995.8%

Reaction Steps

A solution of 7-benzenesulfonyl-2,2-dimethyl-4H-benzo[1,4]oxazin-3-one (0.570 g., 1.79 mmol) in 10 mL freshly distilled THF was cooled to 0° C., and borane-THF complex (5.39 mL of a 1 M solution in THF, 5.39 mmol) was added dropwise over 2 minutes. The resulting solution was warmed to reflux and stirred for 1 hour. Ethanolic hydrogen chloride (4 mL of 2 N solution, 8 mmol) was then added dropwise and the reaction was heated at reflux for an additional hour. The reaction mixture was cooled to room temperature and added to a mixture of 100 mL each ethyl acetate and 10% aqueous sodium bicarbonate. Potassium carbonate was added until the pH of the aqueous phase was roughly 7. The organic layer was separated, washed with 50 mL water and 50 mL brine, dried over sodium sulfate and concentrated in vacuo. The resulting crude oil was purified by flash chromatography (10 to 45% ethyl acetate in hexanes) to give 520 mg (94%) of 7-benzenesulfonyl-2,2-dimethyl-3,4-dihydro-2H-benzo[1,4]oxazine as a white powder. MS: 304 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378415B2
Source datasetuspto-grants-2008_05
ORD IDord-cc1ccbffea0e40ef921f945e68d65492
Source noteuspto-grants-2008_05