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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407257Erstellt: 25. Oktober 2026

Ethyl Acetate → HCID 71150502, Verbindung

https://huagongshe.com/reaction/407257

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktAcetonitrile--water (1/1)HCID 18373917—
Edukt2-(4-Chloro-2-fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 67017493—
EduktMethyl 4-amino-6-chloro-5-fluoro-3-(methylthio)picolinateHCID 86675417—
KatalysatorTriphenylphosphine palladium dichlorideHCID 13169693—
LösungsmittelWaterHCID 962—
ProduktHCID 71150502HCID 71150502—

Reaktionsbedingungen

Temperatur115 °C

Reaktionsschritte

Methyl 4-amino-6-chloro-5-fluoro-3-(methylthio)picolinate (300 mg, 1.2 mmol), 2-(4-chloro-2-fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (450 mg, 1.6 mmol) Cesium fluoride (370 mg, 2.4 mmol) and his (triphenylphosphine) palladium (II) chloride (84 mg, 0.12 mmol) were combined in 5 ml 1:1 acetonitrile-water and heated in a microwave reactor at 115° C. for 30 m. The mixture was shaken with 30 ml ethyl acetate and 10 ml water. The org. phase was washed with 10 ml sat. NaCl, dried (Na2SO3) and evaporated. The residue was chromatographed on silica with a 0-40% ethyl acetate-hexane gradient. The gummy material was stirred with hexane to produce the written compound as a white solid, 60 mg. Mp: 113-117° C. 1H NMR (400 MHz, CDCl3) δ 7.27-7.24 (m, 2H), 5.31 (s, 2H), 3.98 (d, J=1.1 Hz, 3H), 3.96 (s, 3H), 2.32 (s, 3H). 19F NMR (376 MHz, CDCl3) δ −127.97, −128.06, −140.43, −140.52. ESIMS m/z 375 ([M+H]+), 373 ([M−H]−).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754229B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-acb849c9add04051938b958970a7c606
Quellennotizuspto-grants-2014_06