HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-(5-Bromo-4-methylthiophen-2-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Bromo-3-methylthiophene | HCID 84314 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(5-Bromo-4-methylthiophen-2-yl)ethan-1-one | HCID 45480353 | 56.6% |
Reaction Steps
Acetyl chloride (7.09 g) is added to a suspension of AlCl3 (11.53 g) in dichloromethane (310 ml) at 0° C. After 45 minutes at 0° C., 2-bromo-3-methylthiophene (5.0 g) is added dropwise. After 1 hour at 0° C., the reaction is quenched by added water (100 ml). The mixture is extracted three times with dichloromethane. The organic phases are combined, dried over MgSO4 and concentrated in vacuo. The crude product is purified by chromatography on silica gel (180 g) eluting with a mixture of ethyl acetate and heptane (1:6) to yield 1-{5-bromo-4-methyl-thiophen-2-yl}-ethanone (3.5 g) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383659B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-daf0d56ba7ee4564af2947309fd02365 |
| Source note | uspto-grants-2013_02 |