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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201684Generated: October 29, 2026

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

https://huagongshe.com/reaction/2201684

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 numberUS09365498B2
Source datasetuspto-grants-2016_06
ORD IDord-179a158600e14900b8b2b8757bd6eb20
Source noteuspto-grants-2016_06