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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925135Generated: October 28, 2026

Ammonium Chloride → Ethyl 2-(6-chloropyridazin-3-yl)-2,2-difluoroacetate

https://huagongshe.com/reaction/1925135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSelectfluorHCID 2724933—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantEthyl 2-(6-chloropyridazin-3-yl)-2-fluoroacetateHCID 46941482—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(6-chloropyridazin-3-yl)-2,2-difluoroacetateHCID 4694148352.7%

Reaction Steps

To a solution of ethyl 2-(6-chloropyridazin-3-yl)-2-fluoroacetate (36.6 g, 167 mmol) in anhydrous THF (500 mL) was added lithium hexamethyldisilazide (201 ml, 201 mmol) drop-wise at −78° C. After 15 minutes, a solution of Selectfluor (71.2 g, 201 mmol) in DMF (183 mL) was added drop-wise. Upon complete addition, the reaction was allowed to warm to ambient temperature over a 30 min period. Saturated NH4Cl (70 mL) was then added, and THF was removed via rotary evaporation. The resulting residue was diluted with water (500 mL), extracted with Et2O (3×100 mL), dried with MgSO4, filtered, and concentrated to dryness. The resulting material was purified via MPLC (Hex:EtOAc, 8:2) to provide ethyl 2-(6-chloropyridazin-3-yl)-2,2-difluoroacetate 45D (20.8 g, 88 mmol, 52.5%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.25 (t, J=7.07 Hz, 3 H) 4.38 (q, J=7.07 Hz, 2 H) 8.26 (d, J=9.09 Hz, 1 H) 8.33 (d, J=8.84 Hz, 1 H). ESI-MS:m/z 237.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178534B2
Source datasetuspto-grants-2012_05
ORD IDord-4910a37971514e8e891eaa4dd84e79c7
Source noteuspto-grants-2012_05