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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041728Generated: October 26, 2026

Chloral alcoholate → N-(2-chloro-4-fluorophenyl)-2-(N-hydroxyimino)acetamide

https://huagongshe.com/reaction/1041728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloral alcoholateHCID 10587—
ReactantSodium SulfateHCID 24436—
ReactantBenzenamine, 2-chloro-4-fluoro-HCID 75013—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductN-(2-chloro-4-fluorophenyl)-2-(N-hydroxyimino)acetamideHCID 226127913,437%

Reaction Steps

A solution containing NH2OH.HCl (3.2 g, 46 mmol), anhydrous sodium sulphate (13 g, 93 mmol), and 2.2.2-trichloro-1-ethoxy ethanol (4.1 g, 21.2 mmol) in water (60 mL) was added to a solution of 2-chloro-4-fluroaniline (2 g, 0.27 mmol) in 4 M HCl (25 mL). The solution was refluxed for 40 minutes forming a white precipitate in the process. The mixture was cooled to room temperature, extracted with ethyl acetate three times, dried over sodium sulfate, filtered and concentrated in vacuo to provide 2.01 g of N-(2-chloro-4-fluoro-phenyl)-2-((E)-hydroxyimino)-acetamide: 1H NMR (300 MHz, CDCl3) δ 8.8 (bs, 1H), 8.4 (dd, 1H), 7.9 (s, 1H), 7.6 (s, 1H), 7.2 (dd, 1H), 7.0 (ddd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-aa1631e8f3684d9dae27d31f1d491861
Source noteuspto-grants-2013_10