HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258213Generated: October 25, 2026
Hydrochloric Acid → HCID 19737033, compound
https://huagongshe.com/reaction/258213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phenol, 2-(1,1-dimethylethyl)-4-(1,1,3,3-tetramethylbutyl)- | HCID 605573 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19737033 | HCID 19737033 | 26% |
Reaction Steps
2-t-butyl-4-t-octylphenol (140 g, 0.53 mole) was dissolved in 420 ml of absolute ethanol in a 3 L round bottom flask equipped with a water-cooled condenser. Sodium hydroxide (213 g, 5.3 moles) was dissolved in 200 ml water and added while still hot to the solution of phenol. Chloroform (127 g, 1.06 mole) was added in 2 to 3 ml portions over a 1 hour period. The resulting yellow-brown mixture was stirred for 1 hour while it cooled to ambient temperature. The mixture was diluted into 500 ml of 5M hydrochloric acid. The organic layer was isolated in a separatory funnel and dried over anhydrous magnesium sulfate. The mixture was filtered and rotoevaporated to a thick syrup to yield 26% crude product with an IR spectrum having the characteristic aldehyde carbonyl stretching frequency. The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05266283 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-65d6bea4e2d849a89eee1ca1732bf0e7 |
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| Source note | uspto-grants-1993_11 |
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