HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600762Generated: October 29, 2026
Oxalyl chloride → 3-[5-(2-Fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl isocyanate
https://huagongshe.com/reaction/600762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-[5-(2-Fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzamide | HCID 44142326 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[5-(2-Fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl isocyanate | HCID 57822515 | 95% |
Reaction Steps
Oxalyl chloride (2.5 ml, 28.2 mmol, 2.0 eq.) is then added dropwise under N2 to a suspension of 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzamide (Compound A3, 4.0 g, 14.1 mmol) in anhydrous dichloromethane (20 mL) cooled to 0° C. The mixture is slowly heated to reflux and stirred for an additional 6 h. The solvent is removed on a rotary evaporator. The residue is azeotroped with anhydrous dichloromethane (20 mL) and dried under high vacuum for two hours to give 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoyl isocyanate (Compound A4) as a tan solid 4.12 g (95%) which may be used immediately without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902235B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-f05b2624b003425e8aecd69d8918fad0 |
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| Source note | uspto-grants-2011_03 |
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