HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminumhydride → Methyl 3-butyl-1-formylcyclobutane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Dimethyl 3-butylcyclobutane-1,1-dicarboxylate | HCID 69222797 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 3-butyl-1-formylcyclobutane-1-carboxylate | HCID 71416977 | — |
Reaction Steps
To a solution of 3-butyl-cyclobutane-1,1-dicarboxylic acid dimethyl ester (8.37 g, 36.7 mmol) in diethyl ether (300 mL) at −78° C. under a nitrogen atmosphere was added diisobutylaluminum hydride (1.5M in toluene, 49 mL, 73.4 mmol) dropwise. After 2.5 h, the reaction mixture was quenched with saturated aqueous NH4Cl solution (150 mL) then with 1N HCl solution (150 mL). The aqueous phase was extracted with diethyl ether (100 mL×5), was dried (MgSO4) and was evaporated in vacuo to yield the title compound as a clear, colorless oil (7.2 g, 100%) which was used without further purification. MH+199.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07332485B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-942e0f3865bf4dae91336ed209aaf127 |
| Source note | uspto-grants-2008_02 |