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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethoxymethane | HCID 10024 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | N-(5-bromo-2-hydroxymethyl-phenyl)-5-chloro-2-methoxybenzenesulfonamide | HCID 66789377 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 7-bromo-1-(5-chloro-2-methoxy-benzenesulfonyl)-1,4-dihydro-2H-benzo[d][1,3]oxazine | HCID 66789060 | 871% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696200B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-d0be29b3420d48ae9f72a03379a2aaed |
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| Source note | uspto-grants-2010_04 |
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