HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973672Generated: October 29, 2026
Water → 1,3,4-Oxadiazol-2(3H)-one, 5-(4-chlorophenyl)-
https://huagongshe.com/reaction/973672
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 4-Chlorobenzohydrazide | HCID 10816 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,3,4-Oxadiazol-2(3H)-one, 5-(4-chlorophenyl)- | HCID 11116982 | 93.3% |
Reaction Steps
To a suspension of 4-chlorobenzhydrazide (8.53 grams (g), 0.05 mole) in methylene chloride (100 milliliters (ml)), was dropwise added trichloromethyl chloroformate (5.94 g, 0.03 mole). After addition, the reaction mixture was heated to reflux for 2 hours. The reaction was cooled down to room temperature and poured into a mixture of water (500 ml) and hexane (200 ml) and stirred for 10 to 20 min. The resultant precipitate was collected by suction-filtration and was washed with hexane to give a solid product. The product was dried in air at room temperature overnight yielding 5.5 g (60% yield) of 2-(4-chlorophenyl)-1,3,4-oxadiazolin-5one as a solid, m.p. 225°-227° C. NMR and IR spectra showed the desired structure. Without further purification, this product was subjected to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05064845 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-a31978202d9f45f4b7d7740f8b440bc0 |
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| Source note | uspto-grants-1991_11 |
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