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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859059Generated: October 30, 2026

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

https://huagongshe.com/reaction/1859059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Nitro-2-phenyl-benzoxazole-7-yl)-acetonitrileHCID 21253439—
ReactantSulfuric acid hydrate (1:1)HCID 21910475—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Phenyl-6,8-dihydro-oxazolo[5,4-e]indol-7-oneHCID 21253429—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of (6-nitro-2-phenyl-benzoxazole-7-yl)-acetonitrile (66 mg 0.23 mmol) (Starting Material 7) was suspended in concentrated H2SO4 /H2O (1/1, 2 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 (3 mL) heated at reflux was added excess zinc dust (120 mg, 1.85 mmol) portionwise during thirty minutes. The mixture was filtered through a Celite® 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[5,4-e]indol-7-one. (Yield 17 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153634
Source datasetuspto-grants-2000_11
ORD IDord-30904b1c13a741379f37d38216bb8be5
Source noteuspto-grants-2000_11