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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230589Generated: November 2, 2026

Pyridine → 2-Methylsulfinyl-5-(1H-tetrazol-1-yl)benzoic Acid

https://huagongshe.com/reaction/2230589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
Reactant2-Methylthio-5-(1H-tetrazol-1-yl)benzoic AcidHCID 18464518—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Methylsulfinyl-5-(1H-tetrazol-1-yl)benzoic AcidHCID 18464505—

Reaction Steps

Combine 2-methylthio-5-(1H-tetrazol-1-yl)benzoic acid (0.50 g, 2.0 mmol), pyridine (20 mL) and water (20 mL). Cool in an ice bath. Add phenyltrimethylammonium tribromide (0.75 g, 2 mmol) and tetrahydrofuran (20 mL). Warm to ambient temperature. After 1 hour, add a solution a of sodium bisulfite (1 g) in water (1 mL). Extract the reaction mixture with ethyl acetate and then dichloromethane. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give a residue. the title compound. Chromatograph the residue on silica gel eluting sequentially with ethyl acetate and then 10% methanol/ethyl acetate to give methyl 2-methylsulfinyl-5-(1H-tetrazol-1-yl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-dc1b5f50eb82427ca69980233f37a3bc
Source noteuspto-grants-2002_07