HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,3,4-Trimethylpentan-1-ol → 3,3,4-Trimethylpentanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,3,4-Trimethylpentan-1-ol | HCID 12425334 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,3,4-Trimethylpentanal | HCID 12425335 | — |
Reaction Steps
3,3,4-Trimethylpentanol (1 equiv) is dissolved in CH2Cl2. Pyridinium chlorochromate (1.5 equiv) is added and the resulting mixture is stirred at ambient temperature. The liquid is decanted and concentrated by rotary evaporation. The residue is triturated with 1 to 1 diethyl ether/hexane and mixture is filtered and the filtrate is washed with 1 N HCl. The organic layer is dried over Na2SO4, decanted and concentrated. The aldehyde is purified by fractional distillation to yield 3,3,4-trimethylpentanal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06936606B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-c4d859fffe7a41c28f5913316149751e |
| Source note | uspto-grants-2005_08 |