HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330793Generated: October 30, 2026
Acetic Anhydride → 3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid
https://huagongshe.com/reaction/330793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178513298 | HCID 178513298 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid | HCID 7127818 | — |
Reaction Steps
A mixture of 614 g (3.41 mol) of 3-(N-hydroxycarbamimidoyl)benzoic acid, 756 ml (8.0 mol) of acetic anhydride and 2 l of acetic acid is heated at a temperature of 118° C. for 14 hours. The reaction mixture is cooled to 6° C. and filtered off with suction. The residue is taken up in 2 l of water, filtered off with suction and washed well with water. The residue is recrystallised from ethanol/water: 3-(5-methyl-1,2,4-oxadiazol-3-yl)benzoic acid as colourless crystals; m.p. 225°; ESI 205 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877751B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3a4dc34c0aa1491689ac359a7df09a73 |
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| Source note | uspto-grants-2014_11 |
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