HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-[2,2-Dimethyl-4-(4-methylphenyl)oxan-4-yl]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | 2,2-Dimethyl-4-(4-methylphenyl)-4-(prop-2-en-1-yl)oxane | HCID 68314285 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[2,2-Dimethyl-4-(4-methylphenyl)oxan-4-yl]acetaldehyde | HCID 86671426 | 52% |
Reaction Steps
O3 gas was passed through a solution of 2,2-dimethyl-4-(4-methylphenyl)-4-(prop-2-en-1-yl)oxane (1.21 g, 5 mmol) in CH2Cl2 (50 ml) at −78° C. until the solution turned light blue (about 5 min). After additional 5 minutes, the reaction mix was purged with oxygen gas for 15 min before adding triphenylphosphine (2.62 g, 10 mmol). The reaction was stirred at rt for 4 h and concentrated. Purified by normal phase SiO2 chromatography (10 to 60% EtOAc/hexanes) to give 2-[2,2-dimethyl-4-(4-methylphenyl)oxan-4-yl]acetaldehyde as a colorless oil (641 mg, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09044469B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-dcb8f109365043288527d2a2ba21dd2a |
| Source note | uspto-grants-2015_06 |