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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931090Generated: November 1, 2026

Trifluoroacetic acid → 5-Tert-butylpyridin-2-amine

https://huagongshe.com/reaction/1931090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 5-tert-butylpyridin-2-ylcarbamateHCID 66642981—
SolventDichloromethaneHCID 6344—
Product5-Tert-butylpyridin-2-amineHCID 20587962—

Reaction Steps

To a 0° C. solution of Example 59A (1.0 g, 40 mmol) in dichloromethane (3 mL) was added trifluoroacetic acid (3. mL, 40 mmol). The reaction mixture was stirred at ambient temperature for 3 hours then concentrated under reduced pressure. The residue was diluted with ethyl acetate (100 mL) and washed with saturated aqueous NaHCO3. The layers were separated and the aqueous phase was extracted with ethyl acetate (5×100 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to provide the title compound. MS (ESI+) m/z 151 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188135B2
Source datasetuspto-grants-2012_05
ORD IDord-cb5d937d6d6642d18149dea1d4003d09
Source noteuspto-grants-2012_05