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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62677Generated: October 29, 2026

Trifluoroacetic acid → 5-(Cyclopent-1-en-1-yl)-2-nitroaniline

https://huagongshe.com/reaction/62677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl (5-(cyclopent-1-en-1-yl)-2-nitrophenyl)carbamateHCID 71007338—
SolventDichloromethaneHCID 6344—
Product5-(Cyclopent-1-en-1-yl)-2-nitroanilineHCID 8671252387%

Reaction Steps

A solution of tert-butyl (5-(cyclopent-1-en-1-yl)-2-nitrophenyl)carbamate (4.3 g, 14.13 mmol, 1.0 equiv.) in dichloromethane (50 mL) was added TFA (10 mL) at room temperature. The reaction mixture was stirred at room temperature for 2 h. The reaction was then evaporated under reduced pressure. The crude residue was quenched with a saturated solution of sodium bicarbonate. The product was extracted with ethyl acetate, washed with water and brine, dried, filtered and concentrated under reduced pressure. The crude residue was purified by column chromatography (silica gel, 60% EtOAc/hexanes) to give 5-(cyclopent-1-en-1-yl)-2-nitroaniline (2.5 g, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447030B2
Source datasetuspto-grants-2016_09
ORD IDord-c4a94da8cf6543748792f4e310537c78
Source noteuspto-grants-2016_09