HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Phenyl-2-propen-1-yl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-Phenylprop-2-En-1-Ol | HCID 308 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | 2-Bromo-1-methylpyridinium | HCID 818386 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Phenyl-2-propen-1-yl acetate | HCID 7660 | 82% |
Reaction Steps
To a suspended CH2Cl2 (2 ml) solution of 2-bromo-1-methylpyridinium (720 mg, 2.4 mmol) was added a mixture of cinnamyl alcohol (268 mg, 2.0 mmol), acetic acid (120 mg, 2.0 mmol) and tri-n-butylamine (888 mg, 4.8 mmol) in CH2Cl2 (2 ml), and the resulting mixture was refluxed for 3 hours. After evaporation of the solvent, the residue was separated by silica gel column chromatography, and cinnamyl acetate was isolated in 82% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04206310 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-fbbdbf7e4d28439f8c42c9a5d0606676 |
| Source note | uspto-grants-1980_06 |