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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279945Generated: October 31, 2026

Methyl-5'-chloro-2'-methoxy-4-nitro-2-biphenylcarboxylate → 5'-Chloro-2'-methoxy-4-nitro-2-biphenylcarboxylic acid

https://huagongshe.com/reaction/1279945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl-5'-chloro-2'-methoxy-4-nitro-2-biphenylcarboxylateHCID 10829633—
Reactant5'-Fluoro-2'-methoxy-4-nitro-2-biphenylcarboxylic acidHCID 23433602—
Product5'-Chloro-2'-methoxy-4-nitro-2-biphenylcarboxylic acidHCID 2343348695%

Reaction Steps

This compound was prepared in a manner similar to that of 5′-fluoro-2′-methoxy-4-nitro-2-biphenylcarboxylic acid (EXAMPLE 107) from methyl-5′-chloro-2′-methoxy-4-nitro-2-biphenylcarboxylate (0.83 g, 2.6 mmol) to afford 0.75 g (95%) of 5′-chloro-2′-methoxy-4-nitro-2-biphenylcarboxylic acid as a yellow solid. Data for (5′-chloro-2′-methoxy-4-nitro-2-biphenyl)carboxylic acid: 1H NMR (400 MHz, acetone-d6) 8.69 (d, J=2.5, 1H); 8.46 (dd, J=8.3, 2.6, 1H); 7.68 (d, J=8.5, 1H); 7.41 (dd, J=8.9, 2.7, 1H); 7.33 (d, J=2.8, 1H); 7.08 (d, J=8.6, 1H); 3.75 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448405B1
Source datasetuspto-grants-2002_09
ORD IDord-901052a421984109bb64a009653480a3
Source noteuspto-grants-2002_09