HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl (4-bromo-2,5-dimethyl-thiophen-3-yl)-oxo-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | 3-Bromo-2,5-dimethylthiophene | HCID 638585 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl (4-bromo-2,5-dimethyl-thiophen-3-yl)-oxo-acetate | HCID 70818387 | 39.3% |
Reaction Steps
Under a nitrogen atmosphere, aluminium chloride (1.46 g, 11 mmol) was added per portions at 0° C. to a solution of 3-bromo-2,5-dimethylthiophene (17b) (1.05 g, 5.49 mmol) and ethyl chlorooxoacetate (614 μL, 5.5 mmol) in dichloromethane (12 mL). After 2 hours of vigorous stirring, the reaction mixture was slowly hydrolyzed at 0° C. with water. The organic layer was separated, washed with hydrochloric acid aqueous solution 1N, brine, dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 95/5)) to afford the desired keto-ester (17c) as a orange solid (630 mg, 2.16 mmol, 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-2143aba0159240bdbf63960d01126530 |
| Source note | uspto-grants-2016_01 |