HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220063Generated: October 30, 2026
6-Methyl-2-pyridinecarboxaldehyde → 1-(6-Methylpyridin-2-yl)ethanol
https://huagongshe.com/reaction/2220063
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Methyl-2-pyridinecarboxaldehyde | HCID 70737 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(6-Methylpyridin-2-yl)ethanol | HCID 353138 | 100% |
Reaction Steps
To a −60° C. solution of 6-methyl-pyridine-2-carbaldehyde (25 g, 206 mmol) in tetrahydrofuran (200 mL) was added methyl magnesium bromide (200 mL, 1.4 M in tetrahydrofuran/toluene, 1.36 equiv) over 40 minutes. The reaction mixture was slowly warmed to −10° C. over 90 minutes, and then slowly quenched with saturated aqueous ammonium chloride (75 mL). The liquid phase was decanted from the solids and concentrated in vacuo. The resulting residue was dissolved in methylene chloride, dried over magnesium sulfate, and concentrated in vacuo to yield the title compound (28 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07417041B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-c514cf88f4374c6b9016ab91071e4204 |
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| Source note | uspto-grants-2008_08 |
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