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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376407Generated: October 26, 2026

Hydroxyamine hydrochloride → (S)-4-dibenzofuran-2-yl-4-hydroxyimino-2-(2,2,2-trifluoroacetylamino)-butyric acid

https://huagongshe.com/reaction/376407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium Acetate TrihydrateHCID 23665404—
Reactant(S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acidHCID 54131944—
SolventMethanolHCID 887—
Product(S)-4-dibenzofuran-2-yl-4-hydroxyimino-2-(2,2,2-trifluoroacetylamino)-butyric acidHCID 8675509912.7%

Reaction Conditions

Temperature24 °C

Reaction Steps

To a solution of (S)-4-dibenzofuran-2-yl-4-oxo-2,2,2-trifluoroacetylamino)-butyric acid (1.0 g, 0.0026 mol) from Example 1 in 50 mL of methanol was added sodium acetate trihydrate (1.08 g, 0.0079 mol). The solution was stirred at 24° C. while an aqueous solution (5 mL) of hydroxylamine hydrochloride (0.37 g, 0.00527 mol) was added in one portion. The reaction mixture was stirred for 3 hours at 24° C., and then heated to reflux for 2 hours. The solution was cooled to 24° C. and concentrated to dryness by evaporation under reduced pressure. The solid was rinsed with 10 mL of water, and crystallized from ethyl acetate and hexane to afford 0.13 g of (S)-4-dibenzofuran-2-yl-4-hydroxyimino-2-(2,2,2-trifluoroacetylamino)-butyric acid; mp 128-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020366
Source datasetuspto-grants-2000_02
ORD IDord-3a58cdb5eb524fb881f3b36b228bd0ca
Source noteuspto-grants-2000_02