HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-Nitrobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Nitrobenzoic acid | HCID 11087 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (2,6-Dichloropyridin-4-yl)methanol | HCID 2794840 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Nitrobenzoyl chloride | HCID 11875 | — |
Reaction Steps
1.4 g of 2,6-dichloro-4-pyridinemethanol were dissolved into 5 ml of pyridine, and the solution was cooled by ice. To this, 1.5 g of 2-nitrobenzoyl chloride, which was prepared from 2-nitrobenzoic acid and thionyl chloride, were added dropwise. After the reacted solution was stirred for 2 hours, dichloromethane was added. The organic phase was washed with water, and was dried by adding sodium sulfate. The solvent was removed by evaporation, and the residue was purified by silica gel column chromatography to obtain 1.4 g of (2,6-dichloro-4-pyridinyl)methyl 2-nitrobenzoate ester (Compound No. 69).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06281231B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-6fbf19ffc48248c1be633803a49b6825 |
| Source note | uspto-grants-2001_08 |