HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536656Generated: October 28, 2026
Diisobutylaluminumhydride → HCID 58123729, compound
https://huagongshe.com/reaction/536656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 66942372 | HCID 66942372 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58123729 | HCID 58123729 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08859580B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-424e293e0588419aae24ec7ac2ee285f |
|---|
| Source note | uspto-grants-2014_10 |
|---|