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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Indole-5-carbonitrile | HCID 27513 | — |
| Reactant | Methyl 4-(bromomethyl)-3-methoxybenzoate | HCID 2759828 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 4-(5-cyanoindol-3-ylmethyl)-3-methoxybenzoate | HCID 14882553 | 53% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04894386 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-83f0152fe37b4cb6af71cb2d6c9a1f90 |
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| Source note | uspto-grants-1990_01 |
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