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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613208Generated: October 26, 2026

Phenol, 4-(1,1-dimethylethyl)-2-nitro- → 2-Amino-4-tert-butylphenol

https://huagongshe.com/reaction/613208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenol, 4-(1,1-dimethylethyl)-2-nitro-HCID 18661—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-Amino-4-tert-butylphenolHCID 7098281.5%

Reaction Steps

Commercially available 4-t-butyl phenol (30 g, 0.2 mole) was dissolved in 200 mL ethyl acetate in a 600-mL round-bottomed flask fitted with a mechanical stirrer, and cooled to 0° C. The mixture was treated with nitric acid (13 mL, in 13 mL water) dropwise over 10 min and then a catalytic amount of NaNO2. After 45 min the reaction was washed with excess 1N HCl and the organic layer was dried over MgSO4 and stripped to yield 37 g of 2-nitro-4-t-butyl phenol. This nitrophenol (37 g, 0.19 mole) was dissolved in 100 mL ethyl acetate and placed into a Parr bottle with a teaspoon of 10% Pd/C. The mixture was placed on a hydrogenator under 50 psi hydrogen with agitation for 1 hr. The catalyst was filtered off through celite, and the ethyl acetate was stripped off under vacuum. The material crystallized with the addition of about 200 mL heptane to give 25.6 g of the corresponding amine (2-amino-4-t-butyl phenol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06007973
Source datasetuspto-grants-1999_12
ORD IDord-5a785d0f788f4e72a78966f06d5051a7
Source noteuspto-grants-1999_12