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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574086Generated: October 30, 2026

Sodium Methoxide → HCID 86669363, compound

https://huagongshe.com/reaction/574086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant2,3,5-trifluoro-N-(2-fluoro-4-iodophenyl)-6-nitroanilineHCID 57430072—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86669363HCID 86669363—

Reaction Steps

To a solution of 2,3,5-trifluoro-N-(2-fluoro-4-iodophenyl)-6-nitrobenzenamine (Intermediate 12. 700 mg, 1.7 mmol) in THF (20 mL) was added NaOMe solution at −78° C. (which was prepared by dissolving Na metal (39 mg, 1.7 mmol) in 4 mL of methanol). The reaction mixture was brought to rt and stirred for 1 h at same temperature. The progress of reaction was monitored by TLC. After completion, the reaction mixture was quenched with water and extracted with ether. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by flash column chromatography to yield 2,5-difluoro-N-(2-fluoro-4-iodophenyl)-3-methoxy-6-nitrobenzenamine as yellow solid (597 mg). 1H-NMR (400 MHz, CDCl3): δ 3.95 (3H, s), 6.51-6.56 (1H, m), 6.57-6.65 (1H, m), 7.34 (1H, d, J=8.8), 7.42 (1H, dd, J=1.6, 10), 7.7 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034861B2
Source datasetuspto-grants-2015_05
ORD IDord-ad7816d2c0234aa2b32503719067e077
Source noteuspto-grants-2015_05