HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534839Generated: October 29, 2026
Hydride → (3-Chloro-5-(trifluoromethyl)phenyl)methanol
https://huagongshe.com/reaction/534839
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydride | HCID 166653 | — |
| Reactant | Methyl 3-chloro-5-(trifluoromethyl)benzoate | HCID 46311109 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Chloro-5-(trifluoromethyl)phenyl)methanol | HCID 3857254 | 102% |
Reaction Steps
To a stirred solution of methyl 3-chloro-5-(trifluoromethyl)benzoate (Reference Example 29, 2.20 g, 9.22 mmol) in THF (100.0 mL) at −78° C. was added disobutylaluminum hydride solution (28.00 mL, 1.0 M in methylene chloride, 28.00 mmol) and the resulting reaction mixture was stirred at this temperature for 4 h. After this time, the reaction was quenched with 1.0 M hydrochloric acid (100 mL) and warmed to room temperature. The reaction mixture was diluted with ethyl acetate, washed with aqueous 1.0 M hydrochloric acid, water, and saturated sodium chloride, dried (Na2SO4), filtered, concentrated under reduced pressure to provide (3-chloro-5-(trifluoromethyl)phenyl)methanol (1.98 g, >99%) as a brown oil, which was used without further purification or characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853215B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-cb78efaa19254d6baa7b88449fb720a0 |
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| Source note | uspto-grants-2014_10 |
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