HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tempo → 1-[1-[2-(tert-Butyldiphenylsiloxy)ethyl]cyclohexyl]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tempo | HCID 2724126 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | 2-[1-(2-tert-Butyldiphenylsiloxyethyl)cyclohexyl]ethanol | HCID 57427860 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[1-[2-(tert-Butyldiphenylsiloxy)ethyl]cyclohexyl]acetaldehyde | HCID 23109890 | 160.2% |
Reaction Steps
After adding 2,2,6,6-tetramethylpiperidine 1-oxyl free radical (31 mg, 0.20 mmol) to a solution of 2-[1-[2-(tert-butyldiphenylsiloxy)ethyl]cyclohexyl]ethanol (810 mg, 1.97 mmol) and iodobenzene diacetate (700 mg, 2.17 mmol) in methylene chloride (10 mL), the mixture was stirred at room temperature for 4 hours. The reaction mixture was washed with saturated aqueous sodium hydrogencarbonate and saturated brine in that order and dried (anhydrous sodium sulfate), and then the solvent was distilled off under reduced pressure to obtain the title compound as a brown oil (1.29 g). This was used without purification for the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601843B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-e72eb954a3f44f64b8ee325944ed2115 |
| Source note | uspto-grants-2009_10 |