HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl 2,2-dihexylmalonate → 2,2-Dihexylpropane-1,3-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl 2,2-dihexylmalonate | HCID 599758 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2-Dihexylpropane-1,3-diol | HCID 22719291 | — |
Reaction Steps
A suspension of lithium aluminum hydride (LAH) (2 g, 52.6 mmol) in dry THF (20 mL) was stirred at room temperature, and a THF solution of substituted malonic acid diethyl ester (26.3 mmol, (5)) was added dropwise. The reaction was allowed to reflux for 3 h and was quenched by the addition of cold water. The compound was extracted in ethyl acetate. The organic layer was washed with water, dried over Na2SO4, and evaporated to produce the product (6) as either a sticky liquid or a low-melting solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822635B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-64fc795d7941443292bd453da98fec03 |
| Source note | uspto-grants-2014_09 |