HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794081Generated: November 2, 2026
Ethyl Acetate → {6-[(2-Fluorophenyl)methoxy]pyridin-3-yl}methanol
https://huagongshe.com/reaction/1794081
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 6-[(2-Fluorophenyl)methoxy]pyridine-3-carboxylic acid | HCID 22220045 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {6-[(2-Fluorophenyl)methoxy]pyridin-3-yl}methanol | HCID 22220075 | 75% |
Reaction Steps
to a stirred solution of 6-(2-fluorobenzyloxy)nicotinic acid (0.89 g) in THF (10 ml) at 0° C. under Ar was added dropwise a solution of lithium aluminium hydride (1.0 M, 5.5 ml). The mixture was warmed to room temperature and stirred for 2 h. Saturated potassium sodium tartrate solution (1 ml) was added to the mixture followed by ethyl acetate (10 ml). The mixture was stirred for 30 min, filtered and concentrated in vacuo to give the product as a clear oil (0.63 g) which was used without further purification; δH (400 MHz, CDCl3) 8.14 (1H, d, J 1.5 Hz), 7.63 (1H, dd, J 8.5, 2.5 Hz), 7.49 (1H, dt, J 7.5, 1 Hz), 7.29 (1H, m), 7.13 (1H, dt, J 7.5, 1 Hz), 7.02 (1H, dt, J 10, 1 Hz), 6.81 (1H, d, J 8 Hz), 5.45 (2H, s) and 4.63 (2H, s); LC 73%, 2.24 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07022707B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-d39c6df19fb040bc8ffdbe3a44beb477 |
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| Source note | uspto-grants-2006_04 |
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