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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418191Generated: October 31, 2026

Water → 2-t-Butyl-5-cyano-1-nitrobenzene

https://huagongshe.com/reaction/1418191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 19348480HCID 19348480—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-t-Butyl-5-cyano-1-nitrobenzeneHCID 1070336296.5%

Reaction Steps

3.3 ml of pyridine and then 4.3 ml of trifluoroacetic anhydride were added to a solution of 2.25 g (10.1 mmol) of 2-t-butyl-5-carbamoyl-1-nitrobenzene [prepared as described in Preparation 38(i)] in 20 ml of tetrahydrofuran, and the resulting mixture was stirred for 20 minutes. The reaction mixture was then mixed with water, and the aqueous mixture was extracted with a mixture of ethyl acetate and hexane. The extract was washed with water and with a saturated aqueous solution of sodium chloride, after which it was dried over anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through 50 g of silica gel to give 1.99 g (yield 96%) of the title compound as crystals, melting at 70.5°-71.5° C. (from hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880147
Source datasetuspto-grants-1999_03
ORD IDord-8862bac8dfb741eb90d578890d6e8e7e
Source noteuspto-grants-1999_03