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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236123Generated: November 2, 2026

Pyrrolidine → 3-Azulen-1-ylmethylene-1-benzyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2236123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant1-Azulene carboxyaldehydeHCID 11744870—
Reactant1-benzyl-1,3-dihydro-2H-indol-2-oneHCID 11790821—
SolventEthanolHCID 702—
Product3-Azulen-1-ylmethylene-1-benzyl-1,3-dihydro-indol-2-oneHCID 6858303987.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

1-Formylazulene (1 mmol) was dissolved in 20 mL ethanol. 223 mg 1-benzylindolin-2-one (1 mmol) and 20 mL ethanol were then added. Next, a 2 mL solution (1 mmol) containing 1M pyrrolidine and ethanol was added to react at room temperature for three days. After removal of solvent, the resulting solution was extracted by 150 mL ethyl acetate and 50 mL water. The resulting solution was extracted again by 50 mL citric acid aqueous solution and ethyl acetate. The ethyl acetate layer was collected, dried with anhydrous magnesium sulfate, filtered, and concentrated under vacuum. Next, methanol was added and ultrasonically shaken at 40° C. for 1 hour. After filtration, washing by methanol, and drying, Compound 002 (315 mg, 87%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714146B2
Source datasetuspto-grants-2010_05
ORD IDord-e4cbc6c77b6247c0b34c10def7e47f39
Source noteuspto-grants-2010_05