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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635979Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 18673927, compound

https://huagongshe.com/reaction/1635979

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 18673936HCID 18673936—
SolventEthyl AcetateHCID 8857—
ProductHCID 18673927HCID 18673927—

Reaction Conditions

Temperature100 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511995B1
Source datasetuspto-grants-2003_01
ORD IDord-c4fdabee3d2b4242ba6bef47b16076e3
Source noteuspto-grants-2003_01