Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 6-Hydroxy-1H-indole-2-carboxylic acid | HCID 22350191 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68949735 | HCID 68949735 | 90.1% |
Reaction Steps
6-Hydroxy-1H-indole-2-carboxylic acid (5.40 g, 30.48 mmol) is dissolved in THF (100 ml) and imidazole (10.38, 152.4 mmol) is added. The mixture is stirred for 5 minutes, TBDMS-Cl (13.78 g, 91.44 mmol) is added. The reaction is stirred at room temperature for 1 hour. The mixture is filtered into water (200 ml). The solid is washed with THF (50 ml). The filtrate is concentrated to remove THF. The product is extracted with ethyl acetate (100 ml) three times. The organic is dried (MgSO4), filtered, and concentrated to provide 6-(tert-Butyl-dimethyl-silanyloxy)-1H-indole-2-carboxylic acid (8.0 g, 90% yield). 1H NMR (400 MHz, DMSO-d6): δ 12.73 (s, 1H) , 11.43 (s, 1H), 7.49 (d, 1H), 7.00 (s, 1H), 6.84 (s, 1H), 6.63 (m, 1H), 0.97 (s, 9H), 0.20 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439249B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-00cb47dc47c048ecbd80264e0849eb3e |
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| Source note | uspto-grants-2008_10 |
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