HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2,1,3-Benzoxadiazole-5-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2,1,3-Benzoxadiazole-5-carboxylic acid | HCID 2735454 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,1,3-Benzoxadiazole-5-carbonyl chloride | HCID 2735453 | 79.8% |
Reaction Steps
In a 500 ml reactor fitted with mechanical stirring, thermometer, addition funnel, reflux condenser and nitrogen inlet, [2,1,3]-benzoxadiazole-5-carboxylic acid (28 g) was suspended in toluene (245 ml). To this suspension was added thionyl chloride (39.4 g) and DMF (0.35 ml). The resulting mixture was heated to reflux and maintained for 3 hours. A short pass column was installed and toluene was distilled (atmospheric pressure, 124 ml) off to remove excess reagent. After cooling the remaining toluene was distilled off, which resulted in a thick oil. This oil was distilled (90° C., 2 mm Hg) to remove impurities and the product crystallized on standing (79.8% yield), mp: 55-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642633B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-ea41652043a44941983bac7cd24c1e90 |
| Source note | uspto-grants-2014_02 |