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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983208Generated: October 30, 2026

Sodium 4-cyanobenzenesulfinate → 3-Ethyl-2-methylbenzoxazolium 4-Cyanobenzenesulfinate

https://huagongshe.com/reaction/1983208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium 4-cyanobenzenesulfinateHCID 23668300—
ReactantHCID 67174878HCID 67174878—
SolventEthanolHCID 702—
Product3-Ethyl-2-methylbenzoxazolium 4-CyanobenzenesulfinateHCID 2205505746.1%

Reaction Steps

A solution of 3-ethyl-2-methylbenzoxazolium chloride (0.73 g) in ethanol (20 mL) was added to an Erlenmeyer flask containing a magnetically stirred boiling solution of sodium 4-cyanobenzenesulfinate (0.1 g) in anhydrous ethanol (20 mL). The mixture was allowed to cool to room temperature and was then further cooled in an ice bath. The mixture was filtered and the filtrate was concentrated to dryness using a rotary evaporator. The residue was mixed with deionized water and this mixture was extracted with ethyl acetate (2×20 mL). The combined organic extracts were concentrated to dryness using a rotary evaporator. The resultant solid was then dissolved in methylene chloride, filtered and evaporated to dryness using a rotary evaporator to afford 0.08 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541389B2
Source datasetuspto-grants-2009_06
ORD IDord-ef5322217c2847908cf5b2c6e9c9a8b7
Source noteuspto-grants-2009_06