HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 5-Bromo-3-methylthiophene-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-Methyl-2-thiophenecarboxaldehyde | HCID 79911 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Bromo-3-methylthiophene-2-carbaldehyde | HCID 15115407 | — |
Reaction Steps
26 g of 3-methyl-2-thiophenecarboxaldehyde was dissolved in 100 ml of chloroform and the solution was stirred by cooling with ice. 11 ml of bromine was added dropwise thereto. The temperature was elevated to room temperature and the mixture was stirred overnight. About 1 l of ethyl acetate was added thereto and the mixture was washed with water, then with a saturated aqueous sodium hydrogencarbonate solution and finally with a saturated aqueous common salt solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure to give 46.8 g of 5-bromo-3-methyl-2-thiophenecarboxaldehyde in the form of a dark brown solid, which was subjected to the subsequent reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292770 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-ccdef7e55a914e78b3848345dd6f59c7 |
| Source note | uspto-grants-1994_03 |