HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 18673927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 18673936 | HCID 18673936 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18673927 | HCID 18673927 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To 500 mg of 3-acetyloxy-7-[(5-nitro-2-pyridinyl)oxy]-1H-indene, 5 ml of benzoyl chloride and 15 mg of p-toluenesulfonic acid were added and the mixture was stirred at 100° C. After 1.5 hours, ethyl acetate was added to the reaction solution and the solution was washed in turn with a saturated sodium hydrogencarbonate solution and a saturated sodium chloride solution. The solution extracted with ethyl acetate was dried over anhydrous magnesium sulfate and the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (10:1)) to obtain 130 mg of the titled compound as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06511995B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-c4fdabee3d2b4242ba6bef47b16076e3 |
| Source note | uspto-grants-2003_01 |