HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698208Generated: October 27, 2026
Diisobutylaluminum hydride → HCID 59278372, compound
https://huagongshe.com/reaction/1698208
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Methyl 2-bromo-6-methylpyridine-4-carboxylate | HCID 40425123 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59278372 | HCID 59278372 | — |
Reaction Steps
To a chilled (−78° C.) solution of 2-bromo-6-methyl-isonicotinic acid methyl ester (1.90 g, 8.26 mmol) in CH2Cl2 (200 mL) was added a 1 M solution of DIBAH (24.8 mL, 24.8 mmol) in CH2Cl2. The mixture was allowed to warm to room temperature. After 12 hours, the reaction was quenched with saturated aqueous sodium bicarbonate (100 mL). After 5 hours, phases were separated and the aqueous layer was extracted with CH2Cl2 (3×100 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4, filtered and concentrated. The resulting residue was purified by silica gel chromatography eluting with a gradient of 0-100% ethyl acetate in heptane to afford (2-bromo-6-methyl-pyridin-4-yl)-methanol as white solid. MS m/z 202.45 (M+), 204.44 (M+2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08163918B2 |
|---|
| Source dataset | uspto-grants-2012_04 |
|---|
| ORD ID | ord-06ffbbb4f56042b19da6024378543f6f |
|---|
| Source note | uspto-grants-2012_04 |
|---|