HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30656Generated: October 28, 2026
Methanesulfonic Acid → HCID 69206894, compound
https://huagongshe.com/reaction/30656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Acetic acid, (4-nitrophenoxy)-, hydrazide | HCID 156556 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69206894 | HCID 69206894 | 343.3% |
Reaction Steps
A mixture of 2-(4-nitrophenoxy)acetohydrazide (1.10 g), methanesulfonic acid (0.10 g), triethyl orthoformate (2.31 g) and tetrahydrofuran (50 mL) was heated under reflux for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 2-[(4-nitrophenoxy)methyl]-1,3,4-oxadiazole as colorless crystals (0.79 g, yield 69%) from a fraction eluted with hexane-ethyl acetate (1:1, v/v). Recrystallization thereof from ethyl acetate-hexane gave colorless prism crystals. melting point: 125-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423159B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-0b1a1b1a56b54aa8b12a6bb07c40b606 |
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| Source note | uspto-grants-2008_09 |
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