HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrole-3-carboxylic acid → tert-butyl 1H-pyrrole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrole-3-carboxylic acid | HCID 101030 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-butyl 1H-pyrrole-3-carboxylate | HCID 11171190 | — |
Reaction Steps
0.50 g (4.50 mmol) pyrrole-3-carboxylic acid is suspended in 15 ml absolute benzene and boiled under reflux. A solution 4.07 g (18.0 mmol) 90% N,N-dimethylformamidedi-tert-butylacetal in 15 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 saturated NaCl solution. Drying on sodium sulfate, filtration and concentration on the rotary evaporator leave as a crude product a yellow solid which is purified on silica gel by means of column chromatography (flow agent: petroleum ether/ethyl acetate 90:10) 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-64cc34cca8b4475bbcc75cc4b9ed6660 |
| Source note | uspto-grants-2009_10 |