HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vanillin → 4-Formyl-2-methoxyphenyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Formyl-2-methoxyphenyl trifluoromethanesulfonate | HCID 10802962 | 91% |
Reaction Steps
To a mixture of 4-hydroxy-3-methoxybenzaldehyde (10.0 g, 65.7 mmol) and Et3N (13.0 g, 128.7 mmol) in anhydrous DCM (100 mL) was added Tf2O (28.0 g, 99.2 mmol) dropwise at room temperature and the reaction was stirred for 1 hour. The resulting mixture was quenched with water (100 mL) followed by a standard aqueous/EtOAc workup. The residue was purified by silica gel column chromatography (PE:EtOAc=20:1) to give the product as a colorless oil (17.0 g, yield 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946434B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-f6bcfde68bea4970a4e34b95aeeabcff |
| Source note | uspto-grants-2015_02 |