HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15615Generated: October 27, 2026
Sodium 4-cyanobenzenesulfinate → 3-Ethyl-2-methylbenzoxazolium 4-Cyanobenzenesulfinate
https://huagongshe.com/reaction/15615
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium 4-cyanobenzenesulfinate | HCID 23668300 | — |
| Reactant | HCID 67174878 | HCID 67174878 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Ethyl-2-methylbenzoxazolium 4-Cyanobenzenesulfinate | HCID 22055057 | 46.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732633B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-69b11709e8d64591870ee0251b691585 |
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| Source note | uspto-grants-2010_06 |
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