HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939490Generated: October 31, 2026
Methyl 2-Bromo-5-nitrobenzoate → Methyl-5'-chloro-2'-methoxy-4-nitro-2-biphenylcarboxylate
https://huagongshe.com/reaction/1939490
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 2-Bromo-5-nitrobenzoate | HCID 245494 | — |
| Reactant | 5-Chloro-2-methoxyphenylboronic acid | HCID 2735751 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | Methyl-5'-chloro-2'-methoxy-4-nitro-2-biphenylcarboxylate | HCID 10829633 | 55% |
Reaction Steps
Methyl (5'-chloro-2'-methoxy-4-nitro-2-biphenyl)carboxylate (structure 39 of Scheme XI, where R1 =H, R2 =Cl) This compound was prepared in a manner similar to that of methyl-(5'-fluoro-2'-methoxy-4-nitro-2-biphenyl)carboxylate (EXAMPLE 107) from methyl 2-bromo-5-nitrobenzoate (1.25 g, 4.8 mmol, 1.0 equivuiv), tetrakis(triphenylphosphine)palladium (Aldrich: 0.16 g, 0.14 mmol, 2.9 mol %), and 5-chloro-2-methoxyphenylboronic acid (1.30 g, 6.9 mmol, 1.5 equivuiv) to afford 0.85 g (55%) of methyl-5'-chloro-2'-methoxy-4-nitro-2-biphenylcarboxylate as a yellow-orange solid. Data for methyl-5'-chloro-2'-methoxy-4-nitro-2-biphenylcarboxylate: 1H NMR (400 MHz, CDCl3): 8.73 (d, J=2.4, 1 H); 8.38 (dd, J=8.5, 2.5, 1 H); 7.49 (d, J=8.5, 1 H); 7.36 (dd, J=8.7, 2.5, 1 H); 7.23 (d, J=2.5, 1 H); 6.85 (d, J=8.7, 1 H); 3.76 (s, 3 H); 3.70 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05696130 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-49d6f1d8de48447787c8434761e1800a |
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| Source note | uspto-grants-1997_12 |
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