HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597121Generated: October 25, 2026
Hydrochloric Acid → Phenol, 2,6-bis(1,1-dimethylethyl)-4-nitroso-
https://huagongshe.com/reaction/597121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | Phenol, 2,6-bis(1,1-dimethylethyl)-4-nitroso- | HCID 70383 | — |
Reaction Steps
Ethanol (75 ml) was cooled to 15° C and saturated with hydrogen chloride gas. This solution was diluted by addition of another 400 ml of ethanol. To this alcoholic solution was added 82.4 grams of 2,6-di-tert-butylphenol. After it was dissolved, a solution of 30.4 grams of sodium nitrite in 40 ml of water was added at 15°-20° C over a period of one hour with stirring. Stirring was continued for another two hours with the temperature allowed to rise to room temperature. The solution was diluted with 200 ml of water, and the product formed was collected by filtration and washed well with water. The filter cake was then slurried in 300 ml of petroleum ether, filtered, washed with another 100 ml of petroleum ether and dried in a vacuum oven at 70°-80° C to yield the desired intermediate 4-nitroso-2,6-di-tert-butylphenol, melting at 219° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04013621 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-0fa31e1b27f3480587e8e1bb040bd9fc |
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| Source note | uspto-grants-1977_03 |
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