HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468884Generated: October 30, 2026
Diisobutylaluminumhydride → (6-Bromo-4-iodopyridin-3-yl)methanol
https://huagongshe.com/reaction/468884
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 6-bromo-4-iodonicotinate | HCID 86674963 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Bromo-4-iodopyridin-3-yl)methanol | HCID 86674964 | 137% |
Reaction Steps
To a solution of methyl 6-bromo-4-iodonicotinate (500 mg, 1.0 mmol) in methylene chloride (6 mL) cooled at 0° C. was added a 1.0M solution of diisobutylaluminum hydride in tetrahydrofuran (5.85 mL) dropwise over 5 minutes. The reaction mixture was stirred at this temperature for 30 minutes and then quenched by dropwise addition of a 1.0M solution of citric acid in water (1 mL). The reaction mixture was diluted with dichloromethane (20 mL) and washed with water (15 mL). The organic layer was separated, dried over sodium sulfate, filtered, and evaporated in vacuo to afford a residue that was purified by flash chromatography (silica, 12 g, ISCO, 0-50% ethyl acetate in heptane) to afford the title compound as a white solid (430 mg, 90%), which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08623889B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-9e6e9adebce441f79cbea34ea4a14eac |
|---|
| Source note | uspto-grants-2014_01 |
|---|