HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593579Generated: October 27, 2026
Potassium Phosphate, Tribasic → 2-(3-benzyloxy-phenyl)-6-chloro-1H-indole
https://huagongshe.com/reaction/593579
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Boc-6-chloroindole-2-boronic acid | HCID 44119151 | — |
| Reactant | 1-Benzyloxy-3-bromo-pyridine | HCID 67093831 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-benzyloxy-phenyl)-6-chloro-1H-indole | HCID 67093471 | — |
Reaction Steps
A flask is charged with 6-chloro-1-Boc-indole-2-boronic acid (0.839 g, 2.83 mmol), 1-benzyloxy-3-bromo-pyridine (0.500 g, 1.89 mmol), potassium phosphate (1.2 g, 5.67 mmol) and DMF (5 mL). The flask is evacuated and filled with nitrogen thrice and Pd(PPh3)4 (0.164 g, 0.141 mmol) is added. The flask is evacuated and filled with nitrogen thrice again, and heated to 80° C. for 3.5 h. The mixture is then diluted with ethyl acetate and washed with water thrice. The organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is redissolved in DCM (1 mL) and trifluoroacetic acid (2 mL) is added. After 1 h, 4M aqueous NaOH is added and following extraction with DCM, the organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by silica gel flash chromatography (heptane-ethyl acetate, 1:1) to afford 2-(3-benzyloxy-phenyl)-6-chloro-1H-indole as a yellow solid. MS (ESI) m/z 335.07 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242963B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-519fb4524ff74a408b9b1e26c0908091 |
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| Source note | uspto-grants-2016_01 |
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