HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645574Generated: October 29, 2026
Ethyl 2-ethylnicotinate → (2-Ethylpyridin-3-yl)methanol
https://huagongshe.com/reaction/645574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-ethylnicotinate | HCID 14580149 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Ethylpyridin-3-yl)methanol | HCID 19690951 | 69.7% |
Reaction Steps
To a suspension of LiAlH4 (0.83 g, 21.76 mmol) in tetrahydrofuran (50 ml) was added drop wise a solution of 2-ethyl-nicotinic acid ethyl ester (Breitmaier et al, Tetrahedron, 26, 1970, 5907-5910) (3 g, 16.74 mmol) in tetrahydrofuran (25 ml) at −50° C. After addition, the temperature was slowly allowed to increase to 0° C. After 3 h, the reaction was quenched with saturated NH4Cl, filtered and washed with 1M NaHCO3 (50 ml). The aqueous layer was extracted with ethyl acetate (3×50 ml). Combined organic extract were dried (Na2SO4), filtered and concentrated to yield 1.6 g (54%) of product as a yellowish liquid. MS (ESI+) m/z 138 (M+H)+;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07704997B1 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-b3be5e73d03247ec90277355c9537889 |
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| Source note | uspto-grants-2010_04 |
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