HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → [5-(Tert-butyl-dimethyl-silanyloxy)-indol-1-yl]-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-(tert-Butyldimethylsilyloxy)-1H-indole | HCID 22250817 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [5-(Tert-butyl-dimethyl-silanyloxy)-indol-1-yl]-acetic acid ethyl ester | HCID 68822475 | 104% |
Reaction Steps
A suspension of 5-(tert-butyl-dimethyl-silanyloxy)-1H-indole (9.2 g, 37.2 mmol), ethyl bromoacetate (4.79 ml, 40.9 mmol) and cesium carbonate (36.4 g, 111.5 mmol) in DMF (140 ml) was stirred for 3 h at RT. Diethyl ether was added and the mixture was washed with 1N HCl and water, and dried over sodium sulfate. The ether phase was concentrated under reduced pressure to give 12.9 g (quant.) of [5-(tert-butyl-dimethyl-silanyloxy)-indol-1-yl]-acetic acid ethyl ester which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07265149B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-8c20dd66e7bf4a8485001374fddb480e |
| Source note | uspto-grants-2007_09 |