HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899199Generated: October 28, 2026
1-Chloro-3-iodobenzene → HCID 11750293, compound
https://huagongshe.com/reaction/899199
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-3-iodobenzene | HCID 12269 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 69212235 | HCID 69212235 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11750293 | HCID 11750293 | 18% |
Reaction Steps
To a stirred solution of 6-amino-4-(4-chlorophenyl)-1,4-dimethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one (0.09 g, 0.30 mmol) and 1-chloro-3-iodobenzene (0.2 mL, 1.62 mmol) in THF (2 mL) was added Pd2(dba)3 (0.03 g, 0.03 mmol), BINAP (0.03 g, 0.05 mmol), sodium t-butoxide (0.07 g, 0.45 mmol), and 18-crown-6 (0.12 g, 0.45 mmol). The reaction mixture was stirred at room temperature for 2 days, quenched with ammonium chloride solution (sat.) and extracted several times with ethyl acetate. The combined organic layers were dried over magnesium sulfate and concentrated. Flash silica gel column separation with 20% ethyl acetate/hexane followed by trituration with hexane gave the title compound as brown solid (0.02 g, 18%). 1H NMR (DMSO-d6): δ 8.43 (s, 1H), 7.46 (dd, J=6.7, 2.0 Hz, 2H), 7.31 (dd, J=6.8, 2.2 Hz, 2H), 7.28 (m, 2H), 7.10 (d, J=10.5 Hz, 1H), 7.09 (s, 1H), 6.94 (m, 2H), 6.80 (m, 1H), 3.17 (s, 3H), 1.92 (s, 3H); MS (ESI) m/z [M+H]+(413/415); MS (ESI) m/z [M−H]−(411/413); Anal. calcd for C22H18Cl2N2O2: C, 63.93; H, 4.39; N, δ 6.78. Found: C, 62.88; H, 4.72; N, 5.67.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354915B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-8148116096424634b3b6c100807664de |
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| Source note | uspto-grants-2008_04 |
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