Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30987Generated: October 29, 2026

Ethanol → Ethyl (7-hydroxy-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl)acetate

https://huagongshe.com/reaction/30987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant(7-Hydroxy-1,1-dioxo-1,4-dihydro-1lambda6-benzo[1,2,4]thiadiazin-3-yl)-acetic acidHCID 11368865—
ProductEthyl (7-hydroxy-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl)acetateHCID 46942308—

Reaction Conditions

Temperature80 °C

Reaction Steps

EtOH (15 mL) and 150 μL of H2SO4 (conc.) were added into the compound 10c (5.03 mmol) and the mixture was heated to 80° C. for 45 minutes with stirring. The solvent was partially evaporated to half of the original volume under reduced pressure. EtOAc (30 mL) was added and the resulted mixture was washed with H2O (15 mL×3) via extraction. The aqueous layer was back extracted with EtOAc once (60 mL) and the combined organic layer was dried over anhydrous MgSO4, filtered, concentrated to give the desired product (4b) (1.11 g) as a gray solid. This crude material was directly used in next step without further purification. LC-MS: (ESI+) m/e=285.10 [M+1]+ (exact ms: 284.05).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425552B2
Source datasetuspto-grants-2008_09
ORD IDord-c173e85b08924514b3c9533037c98213
Source noteuspto-grants-2008_09