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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641339Generated: October 29, 2026

Diethoxymethane → 7-bromo-1-(5-chloro-2-methoxy-benzenesulfonyl)-1,4-dihydro-2H-benzo[d][1,3]oxazine

https://huagongshe.com/reaction/641339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethoxymethaneHCID 10024—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantN-(5-bromo-2-hydroxymethyl-phenyl)-5-chloro-2-methoxybenzenesulfonamideHCID 66789377—
SolventHeptaneHCID 8900—
Product7-bromo-1-(5-chloro-2-methoxy-benzenesulfonyl)-1,4-dihydro-2H-benzo[d][1,3]oxazineHCID 66789060871%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of N-(5-bromo-2-hydroxymethyl-phenyl)-5-chloro-2-methoxy-benzenesulfonamide (2.51 g, 6.17 mmol), toluene-4-sulfonic acid monohydrate (117 mg, 0.617 mmol), and formaldehyde diethyl acetal (15.5 mL) was heated under reflux at 100° C. for 16 h. After cooling, heptane was added to the suspension, which was stirred for 15 min. The precipitate was collected by filtration and dried to afford 7-bromo-1-(5-chloro-2-methoxy-benzenesulfonyl)-1,4-dihydro-2H-benzo[d][1,3]oxazine (2.25 g, 87%). Off-white solid, MS (ISP)=418.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696200B2
Source datasetuspto-grants-2010_04
ORD IDord-d0be29b3420d48ae9f72a03379a2aaed
Source noteuspto-grants-2010_04