HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451697Generated: October 25, 2026
Catechol → 4-(2,2,2-Trichloro-1-hydroxyethyl)benzene-1,2-diol
https://huagongshe.com/reaction/1451697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2,2-Trichloroacetaldehyde hydrate | HCID 20528376 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(2,2,2-Trichloro-1-hydroxyethyl)benzene-1,2-diol | HCID 14266062 | 52.5% |
Reaction Steps
To the solution of 440 g of 1,2-dihydroxybenzene dissolved in 1L of ethylene dichloride was added 1036 g of trichloroacetaldehyde monohydrate and then the reaction solution was cooled down to 0° C. 102 g of triethylamine was slowly added dropwise thereto. The reaction solution was warmed to normal temperature, stirred for about 20 minutes, heated to 50° C. and then stirred for further 3 hours while maintaining the same temperature. After the reaction is completed, the reaction mixture was distilled under reduced pressure to remove ethylene dichloride. The residue was dissolved in 4L of ethylacetate, washed successively with 2400 ml of 0.5N-aqueous hydrochloric acid solution and 2L of saturated saline solution, dried over anhydrous magnesium sulfate and then distilled under reduced pressure to remove the solvent to obtain 540 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05605895 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-426acbc02cc8425986b270c8c8943021 |
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| Source note | uspto-grants-1997_02 |
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