HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indole-5-Carboxylic Acid → Tert-butyl 1H-indole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indole-5-Carboxylic Acid | HCID 74280 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Tert-butyl 1H-indole-5-carboxylate | HCID 11183550 | — |
Reaction Steps
0.50 g (3.10 mmol) indole-5-carboxylic acid is suspended in 20 ml absolute benzene and heated under reflux. A solution of 2.80 g (12.39 mmol) 90% N,N-dimethylformamidedi-tert-butylacetal in 20 ml absolute benzene is added drop-wise within 30 min. Following another heating under reflux for 30 minutes and subsequent cooling, the reaction mixture is diluted with diethyl ether, washed with 5% sodium carbonate solution and with saturated NaCl solution. Drying on sodium sulfate, filtration and concentration on the rotary evaporator leave as a crude product a yellow oil which is purified on silica gel by means of column chromatography (flow agent: petroleum ether/ethyl acetate 95:5) and yields the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07608633B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-2c05a6bf02d6418890bfbd2d26790750 |
| Source note | uspto-grants-2009_10 |