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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859057Generated: November 2, 2026

(5-Nitro-2-phenyl-benzoxazole4-yl)-acetonitrile → 2-Phenyl-6,8-dihydro-oxazolo[4,5-e]indol-7-one

https://huagongshe.com/reaction/1859057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Nitro-2-phenyl-benzoxazole4-yl)-acetonitrileHCID 15252117—
ReactantSulfuric acid hydrate (1:1)HCID 21910475—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Phenyl-6,8-dihydro-oxazolo[4,5-e]indol-7-oneHCID 21253436—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of (5-nitro-2-phenyl-benzoxazole4-yl)-acetonitrile (1.10 g, 3.98 mmol) (Starting Material 5) was suspended in concentrated H2SO4 /H2O (1/1, 25 mL) and stirred at 100° C. for 30 min. The resulting solution was diluted with water and extracted with ethyl acetate, and the combined organic extracts were dried over anhydrous magnesium sulfate and concentrated in vacuo to give the crude acid. To a solution of the crude acid in acetic acid (10 mL) heated at reflux was added excess zinc dust (1.57 g, 24.2 mmol) portionwise during thirty minutes or until the reaction solution clarified. The mixture was filtered through a Celite® (Fisher Scientific) pad and washed with hot DMF. The solvent was removed in vacuo and residue was suspended and stirred for 30 minutes in 3M hydrochloric acid. The insoluble solid material was collected, washed with water, and air dried to give 2-phenyl-6,8-dihydro-oxazolo[4,5-e]indol-7-one. (Yield 180 mg, 18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153634
Source datasetuspto-grants-2000_11
ORD IDord-7d601a6a0ceb4730a17e1ab75bdac1ba
Source noteuspto-grants-2000_11