HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748351Generated: October 27, 2026
3-Aminophenylboronic acid → 3-(1-trityl-1H-imidazol-4-yl)aniline
https://huagongshe.com/reaction/1748351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminophenylboronic acid | HCID 92269 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Reactant | 4-Bromo-1-trityl-1H-imidazole | HCID 2773274 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(1-trityl-1H-imidazol-4-yl)aniline | HCID 11475113 | 37.5% |
Reaction Steps
(3-Aminophenyl)boronic acid (1.0 g, 7.3 mmol), 4-bromo-1-trityl-1H-imidazole (2.8 g, 7.3 mmol), tri-t-butylphosphonium tetrafluoroborate (424 mg, 1.5 mmol) and KF (1.4 g, 24.1 mmol) are added into dry THF (20 mL) and argon is bubbled through the mixture for 10 min. Tris-(dibenzylideneacetone)dipalladium(0) (669 mg, 0.7 mmol) is added and the reaction mixture is sealed and heated at 60° C. for 16 h. The solid is filtered and the filtrate is diluted with EtOAc (250 mL). The solution is washed with water (3×100 mL), brine (100 mL), dried (Na2SO4) and concentrated. The crude material is purified by flash column chromatography using methanol in CH2Cl2 to afford the title compound (1.1 g, 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150577B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-5b2fd438d4c34952a78e7f59bd411e6e |
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| Source note | uspto-grants-2015_10 |
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