HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Acetyl-5-bromothiophene | HCID 79335 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-one | HCID 1988398 | — |
Reaction Steps
A solution of bromine (2.9 ml, 56.5 mmol) in 30 ml of CH2Cl2 was added dropwise to a solution of 2-acetyl-5-bromothiophene (10 g, 49 mmol), dioxane (55 ml) and ethyl ether (55 ml). The stirring was continued for 1 h and then the reaction medium was poured into a water/ice mixture and extracted with ethyl ether. The organic phase was washed twice with water, dried over magnesium sulfate and concentrated in a rotary evaporator under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05905088 |
| Source dataset | uspto-grants-1999_05 |
| ORD ID | ord-7d6ed3a5327a4f8dbcc39a02b253f676 |
| Source note | uspto-grants-1999_05 |