HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Thiophen-3-yl)ethanone → 2-Bromo-1-(thiophen-3-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Thiophen-3-yl)ethanone | HCID 15116 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Bromo-1-(thiophen-3-yl)ethan-1-one | HCID 2776379 | 85.4% |
Reaction Steps
3-Acetylthiophene (6.3 g, 50 mmol) was dissolved in anhydrous ether (100 ml) and aluminium chloride (catalytic amount) added. Bromine (2.55 ml, 50 mmol) was added dropwise and then stirred for 10 min. The ether was removed under reduced pressure and the residue washed with water. The crude product was recrystallised from petroleum-ether (60°-80° C.) to yield 3-bromoacetylthiophene m.p. 54°-56° C. (8.76 g, 85%), δH (CDCl3) 8.15(1H, dd, H2), 7.55(1H, dd, H4'), 7.35(1H, dd, H5').
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041567 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-80798c9ad9b94d61a032fecf18f227c2 |
| Source note | uspto-grants-1991_08 |