HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990065Generated: October 31, 2026
Nitrogen → 2-(4-Bromophenyl)thiophene-3-carbonitrile
https://huagongshe.com/reaction/1990065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (4-Bromophenyl)boronic acid | HCID 79599 | — |
| Reactant | 2-Iodothiophene-3-carbonitrile | HCID 10977399 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(4-Bromophenyl)thiophene-3-carbonitrile | HCID 57975319 | — |
Reaction Steps
Degass a solution of 2-iodo-thiophene-3-carbonitrile (20 g, 85 mmol), 4-bromobenzeneboronic acid (18.8 g, 94 mmol), potassium carbonate (26 g, 187 mmol) and tetrakis(triphenylphosphine)-palladium (0) (10 g, 8.5 mmol) in a mixture of anhydrous dimethoxyethane (300 mL) and absolute ethanol (150 mL) with Ar or N2 for 15 min and stir for 12 hours at 80° C. Cool the reaction mixture to room temperature, add water (100 ml) and extract the crude product dichloromethane (3×150 mL). Purification by chromatography (hexane-ethyl acetate 10/1) yields 16.3 g (72%) as a white solid: 1H NMR (CDCl3): δ 7.32 (m, 2H), 7.62 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642361B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-3836629298ae4afa8cc807ef58348857 |
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| Source note | uspto-grants-2010_01 |
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