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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407064Generated: October 30, 2026

Hydrochloric Acid → 4-((Z)-(4-(2-fluorobenzyl)-3,4-dihydro-3-oxobenzo[b][1,4]thiazin-2-ylidene)methyl)benzoic acid

https://huagongshe.com/reaction/2407064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 4-FormylbenzoateHCID 15294—
ReactantSodium ethoxideHCID 2723922—
Reactant4-(2-fluorobenzyl)-2H-benzo[b][1,4]thiazin-3(4H)-oneHCID 3244415—
SolventTetrahydrofuranHCID 8028—
Product4-((Z)-(4-(2-fluorobenzyl)-3,4-dihydro-3-oxobenzo[b][1,4]thiazin-2-ylidene)methyl)benzoic acidHCID 5853886176.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-(2-fluorobenzyl)-2H-benzo[b][1,4]thiazin-3(4H)-one (1 g, 3.66 mmole) and methyl 4-formylbenzoate (1.2 g) were dissolved in THF (20 mL) and to the solution was added NaOEt (1 g). The reaction solution was heated at 70 ° C. overnight and aqueous HCl (5%, 10 mL) was added to quench the reaction. The mixture was extracted with EtOAc (50 mL) twice and combined organic layers were dried over anhydrous magnisum sulfate. After filtration, the solvent was removed under vacuum to give 4-((Z)-(4-(2-fluorobenzyl)-3,4-dihydro-3-oxobenzo[b][1,4]thiazin-2-ylidene)methyl)benzoic acid (1.13 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809530B1
Source datasetuspto-grants-2014_08
ORD IDord-aa0c0e4dcb1e4a88a98e1e0dcbc7f53f
Source noteuspto-grants-2014_08