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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548595Generated: October 26, 2026

p-Toluenesulfonic acid → HCID 57691414, compound

https://huagongshe.com/reaction/548595

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,5-HexanedioneHCID 8035—
ReactantPhenylglycine nitrileHCID 76307—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
ProductHCID 57691414HCID 57691414102.1%

Reaction Conditions

Temperature155 °C

Reaction Steps

p-Toluenesulfonic acid (2 mg, 0.16 mmol) and acetonylacetone (2.14 g, 18.7 mmol) were added sequentially to a solution of 2-aminophenylacetonitrile (2.06 g, 15.6 mmol) in toluene (30 mL). The reaction mixture was heated in an oil bath at 155° C. for 1 hour and then allowed to stand at ambient temperature overnight. Acetonylacetone (0.5 mL) and a small amount of p-toluenesulfonic acid were added and the reaction mixture was heated at reflux for 4 hours. The toluene layer was washed sequentially with saturated sodium bicarbonate and water (×2), dried over magnesium sulfate, filtered, and then concentrated under reduced pressure to a dark oil. The oil was purified by prep HPLC (AnaLogix, eluted with a gradient of 10-30% ethyl acetate in hexanes) to provide 3.35 g of 2-(2,5-dimethylpyrrol-1-yl)phenylacetonitrile as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943610B2
Source datasetuspto-grants-2011_05
ORD IDord-b40475f78fa44b38b242a1e3a0993b80
Source noteuspto-grants-2011_05