HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423217Generated: October 30, 2026
Sodium Carbonate → 3-(2-tert-butylphenyl)-1-(phenylsulfonyl)-1H-indole
https://huagongshe.com/reaction/2423217
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1-(phenylsulfonyl)-1H-indol-3-ylboronic acid | HCID 2776217 | — |
| Reactant | 2-(Tert-butyl)phenyl trifluoromethanesulfonate | HCID 18779207 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(2-tert-butylphenyl)-1-(phenylsulfonyl)-1H-indole | HCID 67241937 | 92% |
Reaction Steps
1-(Phenylsulfonyl)-1H-indol-3-ylboronic acid (150.9 mg, 0.501 mmol), 2-tert-butylphenyl trifluoromethanesulfonate (255 mg, 0.902 mmol) and tetrakis(triphenylphosphine)palladium (0) (58 mg, 0.050 mmol) are combined in a septa capped microwave vial and placed under an argon atmosphere. Degassed solutions of 2 M sodium carbonate (0.75 mL, 1.50 mmol) and of dioxane (2.5 mL) were introduced and the vial heated to 150° C. for 15 minutes in a microwave reactor. The cooled reaction mixture was diluted with water and ethyl acetate, the phases separated and the aqueous extracted twice more with ethyl acetate. The combined extracts were washed with water, brine, dried over sodium sulfate, filtered and evaporated. The residue was purified by silica gel chromatography eluting with a gradient of ethyl acetate and hexanes to give 3-(2-tert-butylphenyl)-1-(phenylsulfonyl)-1H-indole (175.8 mg, 92%) as a colorless gummy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960569B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-2feede511ec445e48403e3681e1b83cf |
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| Source note | uspto-grants-2011_06 |
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