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 | Indole-2-carboxylic acid | HCID 72899 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyl 1H-indole-2-carboxylate | HCID 7723355 | — |
Reaction Steps
5 g of N,N′-carbonyldiimidazole are introduced into a solution of 5 g of indole-2-carboxylic acid in 50 ml of dry tetrahydrofuran; after stirring for 12 hours at ambient temperature, 3.7 g of benzyl alcohol are added and the reaction mixture is brought to its reflux temperature; this is maintained for 8 hours, before removing the solvent by distillation under reduced pressure. The residue is dissolved in ethyl acetate and the organic phase is washed with a N aqueous NaOH solution and then dried before evaporation of the solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE037094E1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-8f168226e94144c6b04f8e16f11a70db |
| Source note | uspto-grants-2001_03 |