HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092908Generated: October 26, 2026
Water → 4-Chloro-alpha-(trichloromethyl)benzenemethanol
https://huagongshe.com/reaction/1092908
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trichloroacetic Acid | HCID 6421 | — |
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Sodium Trichloroacetate | HCID 23681045 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-alpha-(trichloromethyl)benzenemethanol | HCID 21417 | — |
Reaction Steps
A mixture of 4-chloro-benzaldehyde (35.5 g) and trichloro acetic acid (61.5 g) in N,N-dimethylformamide (200 ml) is stirred at 30-35° C. Trichloro acetic acid sodium salt (71.5 g) is added in portions over 20 minutes. Occasionally cooling is necessary. The reaction mixture is stirred at 30° C. for 2 hours. Towards the end it becomes viscous and additional N,N-dimethylformamide (150 ml) is charged. The reaction mixture is poured into water (700 ml). The aqueous phase is extracted with ethyl acetate (600 ml). The organic phase is separated, washed with water (300 ml), dried (magnesium sulfate) and evaporated. 2,2,2-Trichloro-1-(4-chloro-phenyl)-ethanol is obtained as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129560B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-01fa141735804517b7c8aab1b4b6387e |
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| Source note | uspto-grants-2012_03 |
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