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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897537Generated: October 31, 2026

Phenylhydrazine → Indenoindole

https://huagongshe.com/reaction/1897537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
Reactant2-IndanoneHCID 11983—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductIndenoindoleHCID 97598—

Reaction Conditions

Temperature85 °C

Reaction Steps

A modified version of the method reported by Okamoto, et al. was employed. Okamoto, T. A.; Kobayashi, S. M.; Yamamoto, H. N., DE1952019, 1970. To a solution of 2-indanone (16.3 g, 123 mmol) in ethanol (80 mL) was added phenyl hydrazine (12.1 mL, 123 mmol) followed by acetic acid (12 drops) at room temperature. While stirring, the solution was warmed to reflux (oil bath at 85° C.) for 15 minutes at which point it was removed from the oil bath and allowed to cool to room temperature. Light yellow needle-like crystals precipitated from the solution. Upon cooling to room temperature, the solution was cooled to 0° C. for 30 minutes. The crystals were filtered via vacuum filtration and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519122B2
Source datasetuspto-grants-2013_08
ORD IDord-024396fb633f481f9298eb974539b4ae
Source noteuspto-grants-2013_08