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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303647Generated: November 3, 2026

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

https://huagongshe.com/reaction/2303647

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylpyridineHCID 19878—
ReactantSodium amideHCID 24533—
SolventN,N-DimethylanilineHCID 949—
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-dimethylaniline and 2.74 g of 4-t-butyl pyridine at rt. The mixture was stirred at 150° C. for 6 h. During this period, 3 more portions of sodium amide (790 mg each) were added. The reaction was cooled down to rt. The mixture was partitioned between ethyl acetate and water. Aqueous layer was extracted with ethyl acetate (3×). The combined organic phase was washed with brine, dried over magnesium sulfate and concentrated. The residue was purified by flash chromatography with 50% ethyl acetate in hexanes followed by 100% ethyl acetate to give 1.68 g of the title compound as a solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-89ab916e492242879f5a1b6575372909
Source noteuspto-grants-2002_08