HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419299Generated: October 31, 2026
Hydrochloric Acid → 4-Chloro-2-(3-trifluoromethyl-phenoxy)-benzyl alcohol
https://huagongshe.com/reaction/2419299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 4-Chloro-2-(3-trifluoromethylphenoxy)-benzoic acid methyl ester | HCID 54008629 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Chloro-2-(3-trifluoromethyl-phenoxy)-benzyl alcohol | HCID 54408113 | — |
Reaction Steps
A solution of 103 g. of 4-chloro-2-(3-trifluoromethyl-phenoxy)-benzoic acid methyl ester in 400 ml. of tetrahydrofuran is added dropwise at reflux over a period of 30 minutes to a solution of 16.2 g. of lithium borohydride in 280 ml. of absolute tetrahydrofuran. The mixture is then cooled to 0° C. and slowly added dropwise to 400 ml. of 3-N aqueous hydrochloric acid. After the addition of 500 ml. of water, the mixture is extracted twice with ether. After evaporation of the ether, there is obtained 4-chloro-2-(3-trifluoromethyl-phenoxy)-benzyl alcohol in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04105664 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-a474ca1400e34e0b8a33889161b3c391 |
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| Source note | uspto-grants-1978_08 |
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