HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344993Generated: October 25, 2026
Diethyl Ether → 3-Ethyl-5-hexylsulfonamido-2-methylbenzoxazolium p-toluenesulfonate
https://huagongshe.com/reaction/344993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl p-methylbenzenesulfonate | HCID 6638 | — |
| Reactant | 5-Hexylsulfonamido-2-methylbenzoxazole | HCID 15051064 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Ethyl-5-hexylsulfonamido-2-methylbenzoxazolium p-toluenesulfonate | HCID 19993452 | 23% |
Reaction Steps
A mixture of 60 grams (0.2 Mol) 5-hexylsulfonamido-2-methylbenzoxazole and 44 grams (0.22 Mol) ethyl p-toluenesulfonate was heated in a round bottom flask at 150° C. for 5 minutes. Upon cooling to room temperature the crude brown mass almost solidified. The product was dissolved in 25 mL methanol and poured into 300 mL diethyl ether with rapid stirring for one hour. The solid precipitate was chilled at 2° C. for 12 hours, then filtered. The tan powder was thoroughly washed with ether and recrystallized from 200 mL hot isopropyl alcohol to yield 23.4 grams (47 mMol, 23% yield) of white crystalline product, m.p.=159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05055387 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-3643c870cb7b4b4b897b06fdf136c84a |
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| Source note | uspto-grants-1991_10 |
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