HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956032Generated: October 25, 2026
Nitric Acid → 4-tert-Butyl-2,6-dinitroanisole
https://huagongshe.com/reaction/1956032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Tert-butyl-1-methoxy-2-nitrobenzene | HCID 4178447 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-tert-Butyl-2,6-dinitroanisole | HCID 4252602 | — |
Reaction Steps
The recovered 2-nitro-4-tertbutylanisole is then again subjected to nitration. Specifically, the 2-nitro-4-tertbutylanisole intermediate is mixed with between 2-9 parts (by volume) organic solvent such as ethylene dichloride. Next is the cooling of the reaction mixture of 2-nitro-4-tertbutylanisole and organic solvent in an ice-water bath to a temperature below 5° C. This is followed by the adding of a mixture of 70% nitric acid and 98% sulfuric acid while maintaining a temperature below 10° C. Following the acid mixture addition, the cooling bath is removed and the temperature of the reaction mixture is increased to 50° C. and maintained there for 2-10 hours to produce 2,6-dinitro-4-tertbutylanisole and a 2,4-dinitrophenol byproduct.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05777168 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-89e60297595a4b0aa0e5980726685be8 |
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| Source note | uspto-grants-1998_07 |
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