HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium iodide → 2-Chloro-3-ethoxyiminomethyl-4-methylsulfonylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | Methyl 2-chloro-3-ethoxyiminomethyl-4-methylsulfonylbenzoate | HCID 54512790 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Chloro-3-ethoxyiminomethyl-4-methylsulfonylbenzoic acid | HCID 54165147 | 89% |
Reaction Steps
A solution of 4.37 g (0.0137 mol) of methyl 2-chloro-3-ethoxyiminomethyl-4-methylsulfonylbenzoate was slowly added dropwise to 7.29 g (0.055 mol) of lithium iodide in 50 ml of dry pyridine. After stirring for 2 hours at reflux, the reaction mixture was cooled and the solvent was removed under reduced pressure. The residue was taken up in water and adjusted to pH=1-2 with dilute hydrochloric acid. The aqueous phase was extracted with ethyl acetate and the combined organic phases were washed with water, dried and concentrated under reduced pressure. 3.70 g of 2-chloro-3-ethoxyiminomethyl-4-methylsulfonylbenzoic acid were obtained. (Yield 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06576596B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-f7115e2b1be940028bfffa6655a5dcaf |
| Source note | uspto-grants-2003_06 |