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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1430449Erstellt: 26. Oktober 2026

Methanesulfonyl chloride → 3-Acetamido-6-chloro-2-fluorobenzyl methanesulfonate

https://huagongshe.com/reaction/1430449

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonyl chlorideHCID 31297—
EduktN-(4-chloro-2-fluoro-3-(hydroxymethyl)phenyl)acetamideHCID 86713625—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Acetamido-6-chloro-2-fluorobenzyl methanesulfonateHCID 8671362691,9%

Reaktionsschritte

A 0° C. of N-(4-chloro-2-fluoro-3-(hydroxymethyl)phenyl)acetamide (1.05 g, 4.82 mmol) and TEA (1.003 mL, 7.24 mmol) in DCM (30 mL) was treated slowly with methanesulfonyl chloride (0.414 mL, 5.31 mmol), warmed to RT and stirred for 2 h. The mixture was treated with satd. NaHCO3, extracted with DCM (2×) and the combined organics were washed with brine, dried over Na2SO4 and concentrated to dryness to afford 3-acetamido-6-chloro-2-fluorobenzyl methanesulfonate (1.31 g, 74% yield) as an off-white solid. MS (ESI) m/z: 296.0 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08940756B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-a61b109aba2a4179a1f8a668c152d659
Quellennotizuspto-grants-2015_01