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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955114Generated: November 2, 2026

Sodium Azide → (S)-N-[[3-[4-Azido-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide

https://huagongshe.com/reaction/1955114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantSodium AcetateHCID 517045—
Reactant(S)-N-[3-[3-Fluoro-4-aminophenyl]-2-oxo-5-oxazolidinyl]methylacetamideHCID 10778218—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product(S)-N-[[3-[4-Azido-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamideHCID 1070882993.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4.0 g(14.96 mmol) of (S)-N-[3-[3-Fluoro-4-aminophenyl]-2-oxo-5-oxazolidinyl]methylacetamide from Example 9 in 40 mL of 6N HCl solution at 0° C. was treated portionwise with 4.12 g(59.84 mmol) of sodium nitrite, followed by stirring at 0° C. for 2 h. The mixture was then treated in several portions with a solution of 1.94 g(29.92 mmol) of sodium azide and 24.52 g(0.30 mol) of sodium acetate in in 50 mL of water. After addition was complete, solution was extracted with ethyl acetate, and the organic layer was dried (Na2SO4) and concentrated in vacuo to afford 4.1 g(93%) of the title compound as a light yellow solid, sufficiently pure for further use. 1H NMR (CDCl3) δ8.22, 7.59, 7.33, 4.72, 4.10, 3.72, 3.40, 1.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124334
Source datasetuspto-grants-2000_09
ORD IDord-3bd32f29fa204163bfe6b2514156419d
Source noteuspto-grants-2000_09