HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Ethyl 5-bromothiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-Thiophenecarboxylic acid, ethyl ester | HCID 79824 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 5-bromothiophene-3-carboxylate | HCID 15293216 | 57.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
20 g (147 mmol) of aluminum chloride are added portionwise to a solution of 10 g (67 mmol) of ethyl thiophene-3-carboxylate in 160 ml of dichloromethane, cooled beforehand to 0° C. The reaction medium is warmed to room temperature and a solution of 4 ml (73 mmol) of bromine in 10 ml of dichloromethane is then added. After reaction for 50 minutes at room temperature, the reaction medium is poured into a water+ice mixture and extracted with dichloromethane. The organic phase is dried over magnesium sulfate, filtered and evaporated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with a 9/1 heptane/ethyl acetate mixture. 9 g (57%) of ethyl 5-bromothiophene-3-carboxylate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022079B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-2e28ad7ba0ff4be389da89efed115e15 |
| Source note | uspto-grants-2011_09 |