HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-(Trifluoromethyl)phenyl)propan-1-ol → 3-[4-(Trifluoromethyl)phenyl]propanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-(Trifluoromethyl)phenyl)propan-1-ol | HCID 22443642 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[4-(Trifluoromethyl)phenyl]propanal | HCID 21683807 | — |
Reaction Steps
To an ice-cooled orange suspension of pyridinium chlorochromate (3.659 g; 16.896 mmol) in anhydrous DCM (20 ml) was added dropwise a solution of 3-(4-trifluoromethyl-phenyl)-propan-1-ol (2.300 g; 11.264 mmol) in anhydrous DCM (35 ml). The resulting black suspension was allowed to warm-up to rt and was stirred under nitrogen for 3 h. The reaction mixture was directly filtered over silicagel using DCM. After concentration to dryness under reduced pressure, the product 3-(4-trifluoromethyl-phenyl)-propionaldehyde was isolated as a pale yellow oil (1.970 g; 86.5%). LC-MS: tR=0.95 min.; [M+H]+: no ionisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188082B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-5a230912feb04f9eb494536f1bf862fe |
| Source note | uspto-grants-2012_05 |