HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248781Generated: October 30, 2026
Hydrochloric Acid → Methyl 4-(5-formyl-1-methylindol-3-ylmethyl)-3-methoxybenzoate
https://huagongshe.com/reaction/2248781
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 4-(5-formylindol-3-ylmethyl)-3-methoxybenzoate | HCID 14882554 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-(5-formyl-1-methylindol-3-ylmethyl)-3-methoxybenzoate | HCID 14882555 | 81% |
Reaction Steps
Sodium hydride (1.23 g of a 60% dispersion in mineral oil) was added to dry N,N-dimethylformamide (100 ml), under an atmosphere of nitrogen. The mixture was cooled in an ice-bath, a solution of methyl 4-(5-formylindol-3-ylmethyl)-3-methoxybenzoate (9.0 g) in N,N-dimethylformamide (20 ml) added slowly, and the mixture stirred for 1 hr. Methyl iodide (4.34 g) was added slowly, stirring continued for 2.5 hr., then the mixture carefully acidified with hydrochloric acid (100 ml) to give an off-white precipitate which was purified by flash chromatography, eluting with 45:50:5 hexane:methylene chloride:ethyl acetate, to give a yellow oil which was crystallized from a mixture of ethyl acetate and hexane to give methyl 4-(5-formyl-1-methylindol-3-ylmethyl)-3-methoxybenzoate (7.6 g, 81%) as an off-white powder: mp 116°-118° C.; partial NMR(250 MHz, DMSO-d6): 3.80 (s, 3H, OCH3), 3.83(s, 3H, NCH3), 3.93(s, 3H, OCH3), 4.11(s, 2H, ArCH2Ar'), 8.12(s, 1H, H4 -indole), 9.96 (s, 1H, CHO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05041460 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-2e99a3c2b519454aa27a5f22664f71d5 |
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| Source note | uspto-grants-1991_08 |
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