HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307916Generated: November 1, 2026
3,4-Dichlorobenzyl chloride → Methyl N-(3,4-dichlorobenzyl)-2-methoxycarbonyl-3-indoleacetate
https://huagongshe.com/reaction/2307916
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorobenzyl chloride | HCID 7609 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | methyl 3-(2-methoxy-2-oxoethyl)-1H-indole-2-carboxylate | HCID 10332197 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl N-(3,4-dichlorobenzyl)-2-methoxycarbonyl-3-indoleacetate | HCID 54370673 | 65.1% |
Reaction Steps
3,4-Dichlorobenzyl chloride (8.2 g) was added to a stirred solution of methyl 2-methoxycarbonyl-3-indoleacetate (6.5 g) and potassium carbonate (8.36 g) in acetonitrile (200 ml) under an atmosphere of argon. The reaction was heated to 80° C. for 24 hours. The reaction was concentrated in vacuo and partitioned between ethyl acetate and water. Combined organic extracts were washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography using 25% ethyl acetate:iso-hexane as eluent to give the product as a white solid (6.95 g, 65%), NMR d (CD3SOCD3) 3.60 (s, 3H), 3.77 (s, 3H), 4.13 (s, 2H), 5.89 (s, 2H), 6.89 (dd, 1H), 7.16 (t, 1H), 7.27 (d, 1H), 7.34 (t, 1H), 7.52 (d, 1H), 7.57 (d, 1H), 7.78 (d, 1H); M/z (+) 406 (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-3cf926484c394417b443da5113a6b4e4 |
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| Source note | uspto-grants-2004_12 |
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