HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Ethyl 3-(4-bromo-2-methylphenyl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Bromo-2-methylbenzaldehyde | HCID 13555150 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | Ethyl 3-(4-bromo-2-methylphenyl)acrylate | HCID 86598121 | — |
Reaction Steps
To a solution of 4-bromo-2-methylbenzaldehyde (1 eq) and triethylphosphonoacetate (1.1 eq) in THF (0.3M) at rt was added dropwise potassium t-butoxide (1.1 eq, 1M, THF). The mixture was stirred at rt 3 h, quenched with HCl 10%, diluted with ether, washed with a NaHCO3 Solution, brine, dried over MgSO4, filtered and concentrated. Flash chromatography (Hexane:EtOAc; 90:10 to 70:30) afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238706B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-b4f52b7b95a945029a9c3f048999b5f6 |
| Source note | uspto-grants-2007_07 |