HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533248Generated: October 29, 2026
Lithium Hydroxide → 1-(3-(1-Naphthyloxy)propyl)-3-((e)-2-phenylvinyl)-1h-indole-2-carboxylic acid
https://huagongshe.com/reaction/533248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Styrylboronic acid | HCID 5702628 | — |
| Reactant | Ethyl 3-bromo-1-(3-(naphthalen-1-yloxy)propyl)-1h-indole-2-carboxylate | HCID 67316935 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-(1-Naphthyloxy)propyl)-3-((e)-2-phenylvinyl)-1h-indole-2-carboxylic acid | HCID 25101664 | — |
Reaction Steps
A mixture of EXAMPLE 31C (100 mg), (E)-styrylboronic acid (39 mg), and bis(triphenylphosphine)palladium(II) dichloride (8 mg) in 7:3:3 dimethoxyethane:ethanol:1N aqueous LiOH (2 mL) was heated under microwave conditions (CEM Discover) at 130° C. for 30 minutes The mixture was quenched with 1NHCl and extracted with ethyl acetate. The extract was dried (Na2SO4), filtered, and concentrated. The concentrate was purified by reverse phaseHPLC (Zorbax SB-C18, 20-100% acetonitrile/water/0.1% trifluoroacetic acid) to afford the title compound. 1H NMR (400 MHz, DMSO-d6) δ 13.59 (br, 1H), 8.24 (m, 1H), 8.15 (d, 1H), 7.94 (m, 1H), 7.87 (m, 1H), 7.69 (d, 1H), 7.59 (m, 2H), 7.53 (m, 2H), 7.46 (m, 1H), 7.40 (m, 3H), 7.28 (m, 3H), 7.21 (m 1H), 6.87 (d, 1H), 4.87 (t, 2H), 4.17 (t, 2H), 2.34 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853209B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-aeac9c21f3b249d5b4c5802c193c153b |
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| Source note | uspto-grants-2014_10 |
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