HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → ethyl 2-(5-methoxy-1H-indol-3-yl)-2-oxoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 9991766 | HCID 9991766 | — |
| Product | ethyl 2-(5-methoxy-1H-indol-3-yl)-2-oxoacetate | HCID 2763354 | — |
Reaction Steps
To a solution 2-(5-methoxy-1H-indol-3-yl)-2-oxoacetyl chloride (14.78 g, 62.20 mmol) in ethanol (144 mL), Et3N (10.40 mL, 74.63 mmol) was added at 0° C. and the resulting yellow suspension was stirred at rt for 1 h. The percipitate was filtered off, washed with cold ethanol and diethylether to yield ethyl 2-(5-methoxy-1H-indol-3-yl)-2-oxoacetate as an orange oil. LC-MS conditions B: tR=0.63 min, [M+H]+=248.13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09303023B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-dcb8ba21a0024d29a3ea987764069aaf |
| Source note | uspto-grants-2016_04 |