HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605261Generated: October 30, 2026
Phosphorus oxychloride → methyl 3-formyl-1H-indole-4-carboxylate
https://huagongshe.com/reaction/1605261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-Methylformanilide | HCID 66737 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | methyl 1H-indole-4-carboxylate | HCID 2733668 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | methyl 3-formyl-1H-indole-4-carboxylate | HCID 12396096 | — |
Reaction Steps
To a stirred mixture of N-methylformanilide (15.6 g) and phosphorus oxychloride (17.7 g) is added ethylene dichloride (75 g ) followed by 4-indolecarboxylic acid methyl ester (17.5 g). The reaction mixture is stirred at room temperature for 1 1/2 hr., then at 45°-50°C for 30 minutes more. The mixture is now poured into a solution of 75 g of sodium acetate in 150 ml of ice-water. More ethylene dichloride is added. The layers are separated and the organic phase is washed with water, dried (Na2SO4) and evaporated under reduced pressure. The residual brown oil is passed through a silica gel column using 3% methanol in chloroform. Concentration of the eluate affords a solid which on recrystallization from benzene affords the pure title compound, mp 135°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03950343 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-b0fae94079674ec1af322f19032d2701 |
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| Source note | uspto-grants-1976_04 |
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