HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 135817451, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 5-Chlorosalicylic Acid | HCID 9447 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Chloro-2-hydroxybenzamide | HCID 348094 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 135817451 | HCID 135817451 | — |
Reaction Steps
40.0 g of 5-chlorosalicyl-amide and 54.0 g of 5-chlorosalicylic acid are boiled under reflux in 400 ml of xylene after addition of 2.5 ml of pyridine. 38 ml of thionyl chloride are added in the course of 2 h, the mixture is stirred for a further 1 h and the solvent is then distilled off under reduced pressure. The residue is suspended in 200 ml of ethanol, filtered off and washed with ethanol. After drying, 6-chloro-2-(5-chloro-2-hydroxyphenyl)benz[e][1,3]oxazin-4-one is obtained as slightly yellow crystals of m.p. 246-248 C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596750B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-9ca7741588f748499e33889402aeb538 |
| Source note | uspto-grants-2003_07 |