HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → Ethyl 3-indolylglyoxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 3-indolylglyoxylate | HCID 101242 | 84.2% |
Reaction Steps
Pyridine (40 mL, 492 mmol) was added in a single portion to a chilled solution (0° C.) of indole (48 g, 410 mmol) in diethyl ether (820 mL). Ethyl chlorooxoacetate (50 mL, 451 mmol) was added dropwise. The resulting suspension was allowed to warm to ambient temperature over a period of 20 hours. The solid was isolated by filtration and washed with diethyl ether. The solid was combined with water (1 L), stirred for 1 hour, and then isolated by filtration to provide 75 g of ethyl (1H-indol-3-yl)(oxo)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138173B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-e538b1bf3a20418aa517a7cf341d7ab0 |
| Source note | uspto-grants-2012_03 |