HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307919Generated: November 1, 2026
3,4-Dichlorobenzyl chloride → Ethyl 3-formyl-N-(3,4-dichlorobenzyl)indole-2-carboxylate
https://huagongshe.com/reaction/2307919
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-Dichlorobenzyl chloride | HCID 7609 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | ethyl 3-formyl-1H-indole-2-carboxylate | HCID 5107764 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-formyl-N-(3,4-dichlorobenzyl)indole-2-carboxylate | HCID 22603427 | 57% |
Reaction Steps
Sodium hydride (488 mg, 60% in mineral oil) was added to a stirred solution of ethyl 3-formylindole-2-carboxylate (2.21 g) in DMF (100 ml) under argon, and reaction stirred at ambient temperature for 25 minutes. 3,4-Dichlorobenzyl chloride (1.71 ml) was then added and the reaction stirred overnight. The reaction mixture was concentrated in vacuo and the residue dissolved in ethyl acetate (80 ml) and washed with water (2×80 ml), dried (MgSO4) and concentrated in vacuo to give a crude residue which was purified by column chromatography using ethyl acetate:iso-hexane as eluent (gradient 5/95-100/0), to give the product as a yellow solid (2.17 g, 57%); NMR d (CD3SOCD3) 1.25 (t, 3H), 4.40 (q, 2H), 5.80 (s, 2H), 7.00 (m, 1H), 7.30-7.50 (m, 3H), 7.55 (m, 1H), 7.65 (m, 1H), 8.35 (m, 1H), 10.48 (s, 1H); M/z (+) 376.4 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06833387B1 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-b0b33f07078e4f5a94fc9e0bb5194042 |
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| Source note | uspto-grants-2004_12 |
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