HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-(Bromoacetyl)-5-chlorothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Acetyl-5-chlorothiophene | HCID 80572 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(Bromoacetyl)-5-chlorothiophene | HCID 2063634 | 43.2% |
Reaction Steps
A solution of bromine (18.90 g, 118 mmol) in chloroform is added to a solution of 2-acetyl-5-chlorothiophene (19.00 g, 118 mmol) in chloroform at 40°-45° C. The reaction mixture is stirred at room temperature for two hours and diluted with water. The organic layer is separated, dried over MgSO4 and concentrated in vacuo to give a solid. The solid is slurried in an ether/hexane solution, filtered and dried to give the title product as a solid (12.20 g, mp 68°-70° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05480902 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-c3a9920f6fd74ed38401012bf093bc09 |
| Source note | uspto-grants-1996_01 |