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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407257Generated: October 26, 2026

Ethyl Acetate → HCID 71150502, compound

https://huagongshe.com/reaction/407257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAcetonitrile--water (1/1)HCID 18373917—
Reactant2-(4-Chloro-2-fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 67017493—
ReactantMethyl 4-amino-6-chloro-5-fluoro-3-(methylthio)picolinateHCID 86675417—
CatalystTriphenylphosphine palladium dichlorideHCID 13169693—
SolventWaterHCID 962—
ProductHCID 71150502HCID 71150502—

Reaction Conditions

Temperature115 °C

Reaction Steps

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]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754229B2
Source datasetuspto-grants-2014_06
ORD IDord-acb849c9add04051938b958970a7c606
Source noteuspto-grants-2014_06