HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914990Generated: November 2, 2026
Benzene, 1-bromo-3-nitro- → 2-[3-(3-Nitrophenyl)prop-2-ynyl]-1,2,3,4-tetrahydroisoquinoline
https://huagongshe.com/reaction/914990
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene, 1-bromo-3-nitro- | HCID 11457 | — |
| Reactant | 2-(Prop-2-yn-1-yl)-1,2,3,4-tetrahydroisoquinoline | HCID 14341294 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-[3-(3-Nitrophenyl)prop-2-ynyl]-1,2,3,4-tetrahydroisoquinoline | HCID 58958232 | 66.1% |
Reaction Steps
To a solution of 81 (2.06 g, 10.2 mmol) in anhydrous triethylamine (30 mL) were sequentially added 1-bromo-3-nitrobenzene (1.83 g, 10.67 mmol), CuI (0.39 g, 2.05 mmol) and Pd(PPh3)4 (1.17 g, 1.0 mmol). The mixture was heated at 90° C. for 1 hour before it was filtered through Celite® and the filtrate was diluted with EtOAc (150 mL). The resulting solution was washed with water (100 mL), brine (100 mL), dried over Na2SO4 and concentrated. The residue was purified via flash silica gel chromatography to provide 93 (1.97 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07265122B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-7263c587ce444de1ae78eb86f7fdb86f |
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| Source note | uspto-grants-2007_09 |
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