HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Bromo-1-thiophen-3-yl-butan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(Thiophen-3-yl)butan-1-one | HCID 20158043 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Bromo-1-thiophen-3-yl-butan-1-one | HCID 59598618 | 60.9% |
Reaction Steps
1-Thiophen-3-yl-butan-1-one (6.7 g. 43 mmol) in 210 mL diethyl ether was cooled to zero degrees C., and 0.6 ml glacial acetic acid was added dropwise, followed by bromine (2.26 ml, 46 mmol) dropwise. The reaction mixture was allowed to warm to room temperature over hours. The reaction mixture was washed the with water, 1 N sodium thiosulfate, brine, and then dried over magnesium sulfate. Solvent was removed under reduced pressure to give an oil which was chromatographed (5% EtOAc/Hexanes) to give 6.1 g 2-Bromo-1-thiophen-3-yl-butan-1-one, 79%, as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008313B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-e823679ea8b443148ec162a13818710a |
| Source note | uspto-grants-2011_08 |