HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → Ethyl 3-bromo-4-chlorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Bromo-4-chlorobenzoic acid | HCID 2735544 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 3-bromo-4-chlorobenzoate | HCID 12594300 | 104.3% |
Reaction Steps
To a solution of 3-bromo-4-chlorobenzoic acid (3.00 g, 12.74 mmol) and cesium carbonate (6.23 g, 19.11 mmol) in acetonitrile (70 mL) was added iodoethane (5.1 mL, 63.7 mmol). The reaction mixture was heated at reflux overnight. After cooling to room temperature, the solution was extracted with ethyl acetate. The organic layer was washed successively with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated. Choromatography on silica gel (biotage, 5% EtOAc in hexane) afforded 3.5 g of ethyl 3-bromo-4-chlorobenzoate (97%). 1H NMR (300 MHz; CDCl3) 1.40 (t, 3H); 4.37 (q, 2H); 7.52 (d, J=8.1 Hz, 1H); 7.91 (dd, J1=8.4 Hz, J2 =1.8 Hz, 1H); 8.28 (d, J=1.8 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06974826B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-e7f5832c99894304b9ab2f53465a88f8 |
| Source note | uspto-grants-2005_12 |