HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929159Generated: October 31, 2026
Tert-Butyl nitrite → 4-m-Tolyloxy-1H-indole-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1929159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 4-(2-Amino-5-methyl-phenoxy)-1H-indole-2-carboxylic acid ethyl ester | HCID 66841523 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-m-Tolyloxy-1H-indole-2-carboxylic acid ethyl ester | HCID 66841702 | — |
Reaction Steps
Tert-butyl nitrite (0.428 ml, 3.609 mmol) is dissolved in 5 ml of dimethylformamide and heated to 65° C. A solution of 135 (1.1 g, 3.609 mmol) in 5 ml of dimethylformamide is added dropwise and the mixture is stirred of additional 10 minutes. The brown solution is cooled to room temperature, diluted with diethyl ether and washed with 2N HCl and brine. The organic layers are dried over sodium sulphate and evaporated. The crude product (930 mg of a brown oil) is further purified by flash-chromatography (hexane/ethyl acetate 7:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08183366B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-9ac4e2f1d60a4c33a2451bd09d88ffdf |
|---|
| Source note | uspto-grants-2012_05 |
|---|