HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769026Generated: October 27, 2026
1,2-Bis(tert-butylsulfonyl)acetylene → HCID 15232946, compound
https://huagongshe.com/reaction/1769026
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Bis(tert-butylsulfonyl)acetylene | HCID 12974252 | — |
| Reactant | 2-Azidomethyl-4-isopropyl-6-methoxysaccharin | HCID 15291091 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 15232946 | HCID 15232946 | — |
Reaction Steps
Di(t-butylsulfonyl)acetylene (1.50 g.) was added to part (75 mL) of the above-described solution of 2-azidomethyl-4-isopropyl-6-methoxysaccharin in benzene. The resulting solution was heated under reflux for 65 hours, then chromatographed on silica gel (Kieselgel 60, 68 g) using first benzene and then cyclohexane-ethyl acetate (90:10, then 85:15, then 75:25) as eluant. The fractions containing the product, which were identified by thin layer chromatography, were combined and recrystallized from benzene-cyclohexane. Pan (0.5 g) of the resulting product (1.5 g, m.r. 204°-205° C., 26% yield for both steps) was recrystallized twice from ethyl acetate affording 2-[4,5-di(t-butylsulfonyl)-1,2,3-triazol-1-yl]methyl-4-isopropyl-6-methoxysaccharin as pale yellow elongated prisms (0.15 g, m.r. 207.5°-209° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380737 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-f59535f1d38f41d2ba39258c71ce6d1a |
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| Source note | uspto-grants-1995_01 |
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