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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829858Generated: October 27, 2026

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

https://huagongshe.com/reaction/1829858

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 numberUS07064152B2
Source datasetuspto-grants-2006_06
ORD IDord-7f6e1045315a4d8a8b84dde7b2d9e5d5
Source noteuspto-grants-2006_06