HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,5-Diphenylpentane-1,5-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,3-Dibenzoylpropane | HCID 80432 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,5-Diphenylpentane-1,5-diol | HCID 226168 | 85% |
Reaction Steps
While cooled by an ice-bath and stirred intensely, 0.0 mol 1,5-diphenyl-1,5-pentandione was added dropwise slowly to a mixture of 3 g LiAlH4 and 100 ml anhydrous tetrahydrofuran. The mixture was heated refluxing for 5 hours, then cooled. Excess LiAlH4 was decomposed with water. After mixing completely the reaction mixture with ethyl acetate, the mixture was filtered, and the filtrate was dried over anhydrous sodium sulfate. The solvent was removed. Column chromatography gave 1,5-diphenyl-1,5-pentanediol as a white solid, and the yield was 85%. mp: 64-67° C. IR spectrum had a strong —OH absorption peak at 3400 cm−1, and had no —CO— absorption peak at about 1700 cm−1. This demonstrated that the reduction reaction was carried out completely.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07388061B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-571f1e2567434e34a1dd1f0803be349d |
| Source note | uspto-grants-2008_06 |