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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424654Generated: October 26, 2026

Hexane → Propan-2-yl 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)picolinate

https://huagongshe.com/reaction/1424654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSulfuryl chlorideHCID 24648—
ReactantIsopropyl 4-(amino)-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoro-picolinateHCID 70497595—
ProductPropan-2-yl 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)picolinateHCID 7049716158%

Reaction Steps

Propan-2-yl 4-amino-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)picolinate (3.065 g, 8.59 mmol) was dissolved in sulfuryl chloride (150 mL). The solution was stirred under nitrogen at room temperature for 8 h. During this time, a white precipitate formed. Hexane (100 mL) was added, and the mixture was stored overnight at −20° C. The product was filtered, washed with hexane and then slurried in EtOAc (100 mL). The organic suspension was neutralized with satd aq NaHCO3 solution, which caused all solids to dissolve. The organic layer was separated and washed with 10% aq NaHSO3 solution and brine, dried (MgSO4), and concentrated under reduced pressure to give a white solid (1.962 g, 58%): mp 109-111° C.; 1H NMR (400 MHz, CDCl3) δ 7.25 (m, 2H), 5.32 (septet, J=6.3 Hz, 1H, CHMe2), 5.07 (br s, 2H), 3.97 (d, JF-H=1.0 Hz, 3H, OMe), 1.40 (d, J=6.3 Hz, 6H, CHMe2); 19F NMR (376 MHz, CDCl3) δ −128.16 (dd, JF-F=33.3 Hz, JF-H=2.5 Hz, phenyl F), −138.35 (d, JF-F=33.4 Hz, pyridine F5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927731B2
Source datasetuspto-grants-2015_01
ORD IDord-0ca3e73c46184896989aebecd8234234
Source noteuspto-grants-2015_01