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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 398086Erstellt: 23. Oktober 2026

2-Chloro-1-fluoro-4-nitrobenzene → 2-chloro-1-(methylsulfanyl)-4-nitrobenzene

https://huagongshe.com/de/reaction/398086

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
EduktSodium methanethiolateHCID 4378561—
KatalysatorSantonoxHCID 7308—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-chloro-1-(methylsulfanyl)-4-nitrobenzeneHCID 1056009452,3%

Reaktionsschritte

To a solution of 4-fluoro-3-chloronitrobenzene (27 g, 156 mmol) in DMF (150 mL) at room temperature was added 5-tert-butyl-4-hydroxy-2-methylphenyl sulfide (100 mg) followed by sodium thiomethoxide (NaSMe) (10 g, 143 mmol) and the reaction was stirred for 6 h. The DMF was removed in vacuo and the residue was partitioned between ether (1 L) and water (1 L). The ether layer was washed with water (1 L) and brine (1 L), dried (MgSO4) and the solvent was removed under reduced pressure. The residue was purified by column chromatography (SiO2; DCM: pentane 1:5 increasing polarity to 3:7) to give the title compound (15.22 g, 49%) as a yellow solid; δH (400 MHz, CDCl3) 2.53 (3H, s), 7.20 (1H, d), 8.09 (1H, dd), 8.20 (1H, d).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610747B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-76eb74a912a34d528fe9645b42d50541
Quellennotizuspto-grants-2003_08