Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Benzene, 1-(chloromethyl)-3,5-dinitro- | HCID 94673 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | 2,3,3-trimethyl-3H-indol-5-yl-acetic acid | HCID 14117637 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | HCID 86589703 | HCID 86589703 | 54% |
Reaction Steps
3,5-Dinitrobenzyl chloride (12.46 g, 57.5 mmol) was added to a solution of 2,3,3-trimethyl-3H-indol-5-yl-acetic acid (2.5 g, 11.5 mmol) with sodium bromide (5.92 g, 57.5 mmol) in sulfolan (10 ml). The reaction was heated at 100° C. for 20 hrs, then cooled to room temperature. The crude reaction mixture was added dropwise to an excess of ethyl acetate and the dark brown solid was filtered OFF and dissolved in dimethylsulfoxide before purification by reverse phase chromatography. The product was isolated as beige solid (54% yield). 1H NMR (d6-DMSO): δH: 8.75 (s, 1H), 8.45 (s, 2H), 7.15 (s, 1H), 6.95 (d, 1H), 6.70 (d, 2H), 5.10 (s, 2H), 3.95 (s, 2H), 3.45 (s, 3H), 1.40 (s, 6H). MALDI-TOF, m/z=398 (M+=398 for C20H20N3O6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662973B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-d963380559a442ea9a4521d29c994e4f |
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| Source note | uspto-grants-2010_02 |
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