Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420749Generated: October 29, 2026

Diisobutylaluminum hydride → HCID 58001782, compound

https://huagongshe.com/reaction/420749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 58001727HCID 58001727—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 58001782HCID 5800178254%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 5-bromo-6-(trifluoromethyl)-3-pyridinecarboxylate (for a synthesis see Preparation 12(b)) (698 mg, 2.457 mmol) in DCM (20 ml) stirred under N2 at 0° C. was added DIBAL-H (1.5 M solution in toluene, 4.91 ml, 7.37 mmol) dropwise. The reaction mixture was stirred at 0° C. for 3 h and at room temperature overnight. The reaction mixture was diluted with MeOH and concentrated under reduced pressure. The residue was treated with a 1N HCl solution and extracted twice with EtOAc. The combined organic phases were dried over anhydrous Na2SO4 and concentrated under reduced. The crude material was purified by Flashmaster chromatography on a 10 g silica gel cartridge using hexane/EtOAc 95:5 as eluent to afford [5-bromo-6-(trifluoromethyl)-3-pyridinyl]methanol (297 mg, 54%) no pure enough to be used in the next step. The title compound was re-purified by preparative HPLC (column XTerra 30×150 mm, gradient elution: 30 to 80% CH3CN/H2O, uv detection 254 nm) to give the title compound (157 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097628B2
Source datasetuspto-grants-2012_01
ORD IDord-ef5373cf364a4846a0aa59b2fd664632
Source noteuspto-grants-2012_01