HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → benzyl 1H-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Indole-2-carboxylic acid | HCID 72899 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyl 1H-indole-2-carboxylate | HCID 7723355 | 84.6% |
Reaction Steps
10.32 g of 2-indolecarboxylic acid in 70 ml of THF are placed in a three-necked flask at RT, 10.38 g of carbonyldiimidazole are added and, after the evolution of gas has ceased, 7.62 g of benzyl alcohol are then added. After refluxing for 5 hours, the mixture is poured into water and extracted with DCM, and the extracts are dried and evaporated. The crystals formed are washed with iPrOH to give 13.62 g of the expected compound: m.p.=136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380230B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-1abefade2e524a32b0f474e866a99830 |
| Source note | uspto-grants-2002_04 |