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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068216Generated: November 1, 2026

4-tert-Butylpyridine → 4-(tert-Butyl)pyridin-2-amine

https://huagongshe.com/reaction/1068216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylpyridineHCID 19878—
ReactantSodium amideHCID 24533—
Product4-(tert-Butyl)pyridin-2-amineHCID 1235194155.2%

Reaction Conditions

Temperature150 °C

Reaction Steps

To 790 mg of sodium amide were added 20 mL of N,N-dimethylanaline and 2.74 g of 4-t-butyl pyridine at r.t. The mixture was stirred at 150° C. for 6 hours. During this period, 3 more portions of sodium amide (790 mg each) were added. The reaction was cooled down to r.t. The mixture was partitioned between EtOAc and water. Aqueous layer was extracted with EtOAc (3×). The combined organic phase was washed with brine, dried over MgSO4 and concentrated. The residue was purified by flash chromatography with 50% EtOAc in hexanes followed by 100% EtOAc to give 1.68 g of the title compound as a solid: 1H NMR (500 MHz, CDCl3) δ1.21 (s, 9H), 4.55 (br, 2H) 6.44 (t, J=1.1 Hz, 1H), 6.62 (dd, J=5.5, 1.8 Hz, 1H), 7.94 (d, J=5.5Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248755B1
Source datasetuspto-grants-2001_06
ORD IDord-3b474fb256b34e6b8d6227696af3e1d6
Source noteuspto-grants-2001_06