HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18230Generated: October 25, 2026
Dimethylformamide → 1,3-dimethyl-1H-indole-2-carbaldehyde
https://huagongshe.com/reaction/18230
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1,3-Dimethylindole | HCID 70130 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-dimethyl-1H-indole-2-carbaldehyde | HCID 2771468 | 91% |
Reaction Steps
To a stirred solution of phosphorus oxychloride (7.0 mL, 75 mmole) in DMF (25 mL) was added dropwise a solution of 1,3-dimethylindole (12.0 g, 83 mmole) in dry DMF (6.0 mL). The reaction was stirred at RT for 2 hr then was poured onto ice. The mixture was basified with a solution of NaOH (13.2 g, 330 mmole) in H2O (44 mL), then was extracted with Et2O (2×50 mL). The combined organic layers were washed with brine, dried (MgSO4), and concentrated under vacuum. Flash chromatography on silica gel (10% ethyl acetate/hexanes) gave the title compound (13.03 g, 91%) as an off-white solid: LCMS (ES) m/e 174.2 (M+H)+; 1H NMR (400 MHz, CDCl3) δ 10.16 (s, 1 H), 7.68 (d, J=8.1 Hz, 1 H), 7.42 (t, 1 H), 7.32 (d, J=8.5 Hz, 1 H), 7.15 (t, 1 H), 4.04 (s, 3 H), 2.63 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741339B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-3f04ccf34edf418c976cb5f491c86aaa |
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| Source note | uspto-grants-2010_06 |
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