HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101403Generated: October 30, 2026
Ethyl Acetate → (2-Cyclopropyl-6-(trifluoromethyl)pyridin-3-yl)methanol
https://huagongshe.com/reaction/2101403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 2-cyclopropyl-6-(trifluoromethyl)nicotinate | HCID 59834808 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Cyclopropyl-6-(trifluoromethyl)pyridin-3-yl)methanol | HCID 59834793 | 100.4% |
Reaction Steps
To a solution of methyl 2-cyclopropyl-6-(trifluoromethyl)nicotinate (1 g, 4.08 mmol) in THF (6 mL) at 0° C. under argon was added 1.0 M lithium aluminum hydride in THF solution (6 mL, 6.0 mmol). The reaction mixture was stirred at 0° C. for 15 min. EtOAc (20 mL) was added to the reaction mixture, which was then stirred at room temperature for 30 min. A 10% aqueous potassium sodium tartrate solution (20 mL) was added to the reaction mixture and stirring was continued for another 30 min. The organic layer was separated, washed with brine, dried (MgSO4), filtered and concentrated to obtain 890 mg of the title compound as a pale yellow oil. HPLC/MS: retention time=3.055 min, [M+H]+=218.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572808B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-988b2c38f04d4acea65d28588dfcd30e |
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| Source note | uspto-grants-2009_08 |
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