HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33281Generated: October 26, 2026
Sodium Hydroxide → methyl 3-formyl-1H-indole-4-carboxylate
https://huagongshe.com/reaction/33281
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | methyl 1H-indole-4-carboxylate | HCID 2733668 | — |
| Reactant | DMF Phosphorus oxychloride | HCID 13765457 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | methyl 3-formyl-1H-indole-4-carboxylate | HCID 12396096 | — |
Reaction Steps
A solution of methyl indole-4-carboxylate (250 mg, 1.43 mmol) in dichloroethane (2 mL) was treated with a solution of POCl3-DMF (1.5 equivalent (eq)) at room temperature (rt). The orange solution was heated at 50° C. for 1 hour. The reaction solution was poured into ice-cold aqueous (aq.) NaOAc (1 g in 2 mL), the aqueous solution was adjusted to pH=8 with 1M NaOH, and extracted with EtOAc (10 mL×3). The organic solution was washed with water and brine, dried (Na2SO4), filtered, and concentrated to give methyl 3-formyl-indole-4-carboxylate as an oil, 271 mg (93%). 1H NMR (300 MHz, d6-DMSO) δ 3.68 (s, 3H), 7.16 (t, 1H, J=7.8 Hz), 7.40 (dd, 1H, J=7.8, 0.8 Hz), 7.56 (d, 1H, J=7.8, 0.8 Hz), 8.16 (d, 1H, J=3.2 Hz), 10.00 (s, 1H), 12.30 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429578B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-bb23c307690b48c8b2b7e1c1418720d0 |
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| Source note | uspto-grants-2008_09 |
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