HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821940Generated: October 31, 2026
Dimethylformamide → 1H-Indole-3-carboxylic acid, 1,1-dimethylethyl ester
https://huagongshe.com/reaction/1821940
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Indole-3-Carboxylic Acid | HCID 69867 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1H-Indole-3-carboxylic acid, 1,1-dimethylethyl ester | HCID 12308173 | — |
Reaction Steps
1.00 g (6.21 mmol) indole-3-carboxylic acid is dissolved in 150 ml absolute THF, mixed with 0.05 g (0.68 mmol) absolute DMF as well as with 1.48 g (12.5 mmol) thionylchloride and stirred at room temperature for 1 hour. Following the drop-wise addition of 2.51 g (24.8 mmol) tiethylamine and of 9.20 g (124 mmol) tert-butanol and heating under reflux for 2 hours, hydrolysis of the cooled reaction mixture is carried out in water. Three extractions with diethyl ether, concentration to half the volume on the rotary evaporator, washing with 5% sodium carbonate solution and with saturated NaCl solution, drying on sodium sulfate, filtration and reconcentration on the rotary evaporator leave as a crude product a brown oil 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 yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07608633B2 |
|---|
| Source dataset | uspto-grants-2009_10 |
|---|
| ORD ID | ord-a89170fd7bf2434eaa362f3f426f8efe |
|---|
| Source note | uspto-grants-2009_10 |
|---|