HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616670Generated: October 30, 2026
Diisobutylaluminumhydride → 2-Benzyl-2-aza-bicyclo[3.3.1]nonan-6-ol
https://huagongshe.com/reaction/1616670
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 66942372 | HCID 66942372 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Benzyl-2-aza-bicyclo[3.3.1]nonan-6-ol | HCID 58123729 | — |
Reaction Steps
Diisobutylaluminum hydride (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 diisobutylaluminum hydride (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765780B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-1d1645c3e55a4adc8aa275eca92bcd20 |
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| Source note | uspto-grants-2014_07 |
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