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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330171Generated: October 29, 2026

Ethyl Acetate → Methyl 4-(5-cyanoindol-3-ylmethyl)-3-methoxybenzoate

https://huagongshe.com/reaction/330171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantIndole-5-carbonitrileHCID 27513—
ReactantMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
CatalystHCID 178418647HCID 178418647—
SolventTolueneHCID 1140—
ProductMethyl 4-(5-cyanoindol-3-ylmethyl)-3-methoxybenzoateHCID 1488255353%

Reaction Steps

A mixture of 5-cyanoindole (10 g) and freshly prepared silver carbonate on diatomaceous earth (40.66 g) was stirred and heated under reflux in toluene (100 ml) for 18 hr, under an atmosphere of nitrogen. The mixture was cooled to room temperature, methyl 4-bromomethyl-3-methoxybenzoate (22.7 g) added, and stirring continued for 4 hr. Ethyl acetate (200 ml) was added, the mixture filtered through diatomaceous earth, the filter pad washed with ethyl acetate and the filtrate evaporated. The dark oil obtained was purified by flash chromatography, eluting with 45:45:10 hexane:methylene chloride:ethyl acetate, to give a foam which was crystallized from toluene to give methyl 4-(5-cyanoindol-3-ylmethyl)-3-methoxybenzoate (11.8 g, 53%) as white crystals; mp 148°-149°; partial NMR (250 MHz, DMSO-d6): 3.83(s, 3H, OCH3), 3.91(s, 3H, OCH3), 4.08(s, 2H, ArCH2Ar'), 8.00(s, 1H, H4 -indole), 11.49(br s, 1H, H1 -indole).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04894386
Source datasetuspto-grants-1990_01
ORD IDord-83f0152fe37b4cb6af71cb2d6c9a1f90
Source noteuspto-grants-1990_01