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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052094Generated: October 26, 2026

Water → benzyl 1H-indole-3-carboxylate

https://huagongshe.com/reaction/1052094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
ReactantIndole-3-Carboxylic AcidHCID 69867—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productbenzyl 1H-indole-3-carboxylateHCID 8605861—

Reaction Steps

To a solution of 1H-indole-3-carboxylic acid (5 g, 31 mmol) in DMF (70 mL) under a nitrogen atmosphere at 0° C. was added cesium carbonate (11 g, 31 mmol) and benzyl bromide (4.05 mL, 34.1 mmol). The reaction mixture was stirred at RT for 48 h and poured into water. EtOAc was added and the layers were separated and the aqueous layer was extracted with EtOAc (×3). The combined organic layers were washed with water, dried over Na2SO4, filtered and concentrated. The residue was taken up in Et2O and the resulting precipitate was filtered-off to give the title compound. TLC, Rf (c-hexane/EtOAc 1:1)=0.55; MS (LC-MS): 252.1 [M+H]+, 274.0 [M+Na]+, 525.1 [2M+Na]+, 250.1 [M−H]−; tR (HPLC conditions a) 3.77 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388199B2
Source datasetuspto-grants-2016_07
ORD IDord-46af06467be4498280e557a7010e17ea
Source noteuspto-grants-2016_07