HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aspirin → 2-Acetyloxybenzoic acid 6-(chloromethyl)-2methylpyridinyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aspirin | HCID 2244 | — |
| Reactant | 2,6-Bis(chloromethyl)pyridine | HCID 316654 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Acetyloxybenzoic acid 6-(chloromethyl)-2methylpyridinyl ester | HCID 68880764 | 59.9% |
Reaction Steps
To a solution of acetylsalicylic 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 it is diluted with ethyl ether and washed with water. The separated organic phases are anhydrified with sodium sulphate and the solvent is evaporated at a reduced pressure. The reaction raw product is purified by chromatography on silica gel 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 | US07629368B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-a6f008d8cf7f40479d062c5b4a69b1bf |
| Source note | uspto-grants-2009_12 |