HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → 3-(2-Bromoethoxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(2-Bromoethoxy)benzaldehyde | HCID 2735565 | — |
Reaction Steps
A mixture of 3-hydroxybenzaldehyde (5.17 g, 42.33 mmol), K2CO3 (58.5 g) and CH3CN (100 ml) was stirred at room temperature for 15 minutes, then dibromoethane (18.3 ml) was added. The reaction mixture was stirred at room temperature for 30 minutes, then at reflux for 3-4 hours. Additional dibromoethane was added and then the reaction mixture was refluxed overnight. The reaction mixture was cooled, filtered, and the filtrate was stripped to afford an oil. The oil was dissolved in ether (300 ml), washed with 5N NaOH (2×75 ml) and the ether layer was dried over MgSO4 and stripped. The residue was purified by column chromatography on silica gel eluting with 10% ethyl acetate/hexane to afford 5.23 g of 3-(2-bromoethoxy)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958929 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-906f685a24c447c887bf4cd3a385dd1f |
| Source note | uspto-grants-1999_09 |