HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-(6-Methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 6-Methyl-1H-pyrrolo[2,3-b]pyridine | HCID 11457716 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 1-(6-Methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)ethan-1-one | HCID 68308656 | — |
Reaction Steps
To a solution of 6-methyl-1H-pyrrolo[2,3-b]pyridine (500 mg) in dichloroethane (6 mL) were added aluminum chloride (1.09 g) and acetyl chloride (0.40 mL), and then the mixture was stirred at room temperature for 1.5 hours. The reaction solution was poured into aqueous saturated sodium hydrogen carbonate solution, and extracted with chloroform. The organic layer was washed with saturated saline, dried over magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was triturated with isopropyl ether to 1-(6-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone [REx(8-1)] (481 mg) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278944B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-b6a6fd5c48e14501bfbf662271d3427f |
| Source note | uspto-grants-2016_03 |