HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-(Acetyloxy)-5-tert-butylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-(1,1-Dimethylethyl)salicylic acid | HCID 85281 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Acetyloxy)-5-tert-butylbenzoic acid | HCID 12274488 | — |
Reaction Steps
Pyridine (0.034 mL) and acetic anhydride (0.034 mL) were sequentially added to a methylene chloride (0.54 mL) solution of 5-tert-butylsalicylic acid (0.054 g), followed by stirring at room temperature for 2 hours. The solvent was evaporated under reduced pressure, and 1 mol/L hydrochloric acid and ethyl acetate were added to the residue. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 100-90% chloroform/methanol] to obtain 0.049 g of 2-acetoxy-5-tert-butylbenzoic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492582B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-393bfbc670f34754be83d7d354a19086 |
| Source note | uspto-grants-2013_07 |