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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74245Generated: October 29, 2026

2-(4-n-Butylamino-3-nitrophenyl)benzoxazole → 2-(2-n-Butylaminoanilin-5-yl)benzoxazole

https://huagongshe.com/reaction/74245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-n-Butylamino-3-nitrophenyl)benzoxazoleHCID 67498473—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
Product2-(2-n-Butylaminoanilin-5-yl)benzoxazoleHCID 6749885196%

Reaction Steps

To a tetrahydrofuran solution (5 mL) of 2-(4-n-butylamino-3-nitrophenyl)benzoxazole (see Working Example 74-1) (353 mg, 1.13 mmol) was added 10% palladium-carbon (50 mg), a hydrogen atmosphere was substituted in the flask, and this was stirred at room temperature for 15 hours. After the reaction was complete, this was filtered through Celite and the filtrate was concentrated. The residue obtained was purified by silica gel column chromatography to yield the title compound (305 mg, 96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-af1524baa09746e5a53c1f3415b04052
Source noteuspto-grants-2014_09