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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097899Generated: October 31, 2026

Diisobutylaluminum hydride → 3-(2-Chloro-4-hydroxymethyl-phenyl)-2-(2-chloro-pyridin-4-yl)-1,1,1-trifluoro-butan-2-ol

https://huagongshe.com/reaction/1097899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant3-Chloro-4-[2-(2-chloro-pyridin-4-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-benzoic acid methyl esterHCID 57421266—
SolventDichloromethaneHCID 6344—
Product3-(2-Chloro-4-hydroxymethyl-phenyl)-2-(2-chloro-pyridin-4-yl)-1,1,1-trifluoro-butan-2-olHCID 2525444944%

Reaction Conditions

Temperature-15 °C

Reaction Steps

3-Chloro-4-[2-(2-chloro-pyridin-4-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-benzoic acid methyl ester (488 mg, Example 135) was dissolved in CH2Cl2 under argon. The solution was cooled to −15° C. in an ice/salt bath and a solution of DIBAL-H (1M in CH2Cl2, 3 mL) was added drop wise. Stirring was continued and the mixture was allowed to warm to 0° C. over a period of 2 hours. The mixture was then poured into ice/water and extracted with ethyl acetate. The organic extracts were washed with brine, dried over Na2SO4 and evaporated. The residue was purified by flash chromatography (silica gel, gradient of ethyl acetate in heptane) to give the title compound as a colorless solid (200 mg). MS (m/e)=380.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143280B2
Source datasetuspto-grants-2012_03
ORD IDord-8796f6ee3acc4f9db1c27ba2cecfd7bc
Source noteuspto-grants-2012_03