HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21736Generated: October 29, 2026
2',3',4'-Trichloroacetophenone → 1-(2,3,4-Trichlorophenyl)ethan-1-ol
https://huagongshe.com/reaction/21736
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2',3',4'-Trichloroacetophenone | HCID 26132 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(2,3,4-Trichlorophenyl)ethan-1-ol | HCID 16769105 | 99.4% |
Reaction Steps
In methanol (284 ml)is suspended 2',3',4'-trichloroacetophenone (94.7 g), and thereto is added sodium borohydride (7.6 g) at 15° C.-25° C. The mixture is stirred at 25° C. for two hours, and evaporated to remove the methanol. To the residue is added 2N hydrochloric acid (110 ml), and the mixture is extracted with ethyl acetate. The organic layer is washed with water, dried, and evaporated to remove the solvent to give crude 1-(2,3,4-trichlorophenyl)ethanol (95 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05424446 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-04631bac06bc4c08aad218d874f15c39 |
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| Source note | uspto-grants-1995_06 |
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