HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylic Acid → 2-Acetyloxybenzoic acid 6-(chloromethyl)-2methylpyridinyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2,6-Bis(chloromethyl)pyridine | HCID 316654 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Acetyloxybenzoic acid 6-(chloromethyl)-2methylpyridinyl ester | HCID 68880764 | — |
Reaction Steps
To a solution of salicylic acid (1.6 g, 8.88 mmoles) in N,N′-dimethylformamide (20 ml) and under stirring sodium ethylate (0.64 g, 8.88 mmoles) is added. After 30 minutes the obtained solution is added to a solution of 2,6-bis-(chloromethyl)pyridine (4.72 g, 26.81 mmoles) in N,N′-dimethylformamide (20 ml). The solution is left at room temperature for 7 days, under stirring, then is diluted with ethyl ether and washed with water. The separated organic phases are anhydrified with sodium sulphate and the solvent is evaporated at reduced pressure. The reaction crude product is purified by chromatography on silica gel by eluting with n-hexane/ethyl acetate 7/3. 1.7 g of the product as yellow oil are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06613784B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-b05a90314d204242a2ac14f8fc776bbd |
| Source note | uspto-grants-2003_09 |