HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613207Generated: October 27, 2026
Nitric Acid → Phenol, 4-(1,1-dimethylethyl)-2-nitro-
https://huagongshe.com/reaction/613207
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Phenol, 4-(1,1-dimethylethyl)-2-nitro- | HCID 18661 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06007973 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-1810989357024d50a67177fb9b005512 |
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| Source note | uspto-grants-1999_12 |
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