HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912699Generated: October 31, 2026
Sodium borohydride → 6-Butoxy-2-hydroxymethylpyridine
https://huagongshe.com/reaction/912699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 6-butoxypyridine-2-carboxylate | HCID 67415067 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Butoxy-2-hydroxymethylpyridine | HCID 19756116 | 91% |
Reaction Steps
Methyl 6-butoxypyridine-2-carboxylate (2.46 g, 11.8 mmol, obtained from Example 17(b)) was dissolved in absolute ethanol (112 mL) and sodium borohydride (1.78 g, 47.0 mmol, 4 equiv.) was added. After refluxing for 1 h, another 2 equivalents of sodium borohydride were added and then after 2 h more an additional 2 equivalents more sodium borohydride were added. After another 3 h the reaction was cooled to r.t. and concentrated in vacuo. The residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo producing 1.92 g (91% yield, 10.7 mmol) of the title compound as a clear liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08026244B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
|---|
| ORD ID | ord-521de58ff919405e8aedb28e2ae56921 |
|---|
| Source note | uspto-grants-2011_09 |
|---|