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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531145Generated: October 31, 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/1531145

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 numberUS06197804B1
Source datasetuspto-grants-2001_03
ORD IDord-7f88432616934a509f56c33efe5776ee
Source noteuspto-grants-2001_03