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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536656Generated: October 28, 2026

Diisobutylaluminumhydride → HCID 58123729, compound

https://huagongshe.com/reaction/536656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 66942372HCID 66942372—
SolventTolueneHCID 1140—
ProductHCID 58123729HCID 58123729—

Reaction Conditions

Temperature-70 °C

Reaction Steps

Diisobutylaluminumhydride (1.5 mol/L in toluene, 21 mL) is added to a solution of acetic acid 2-benzyl-3-oxo-2-aza-bicyclo[3.3.1]non-6-yl ester (1.50 g, for synthesis see J. Chem. Soc., Perkin Trans. 1 1999, 1157-1162) in toluene (30 mL) cooled to −70° C. The cooling bath is removed and the solution is stirred at ambient temperature overnight. Then, another portion of diisobutylaluminumhydride (1.5 mol/L in toluene, 20 mL) is added and the solution is stirred for additional 4 h at room temperature. Then, the solution is poured into ice-cold water and the resulting mixture is extracted with ethyl acetate. The aqueous phase is acidified using 4 M hydrochloric acid and extracted one more time with ethyl acetate. The combined organic extracts are dried (Na2SO4) and the solvent is removed. The residue is purified by chromatography on silica gel (dichloromethane/methanol 1:0->2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859580B2
Source datasetuspto-grants-2014_10
ORD IDord-424e293e0588419aae24ec7ac2ee285f
Source noteuspto-grants-2014_10