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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531588Generated: November 1, 2026

Benzyl Alcohol → benzyl 1H-indole-2-carboxylate

https://huagongshe.com/reaction/1531588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantIndole-2-carboxylic acidHCID 72899—
SolventTetrahydrofuranHCID 8028—
Productbenzyl 1H-indole-2-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037094E1
Source datasetuspto-grants-2001_03
ORD IDord-8f168226e94144c6b04f8e16f11a70db
Source noteuspto-grants-2001_03