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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852590Generated: October 31, 2026

Hydrogen Bromide → Methyl 5-bromo-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoate

https://huagongshe.com/reaction/852590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium NitriteHCID 23668193—
ReactantMethyl 5-amino-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoateHCID 69357536—
ProductMethyl 5-bromo-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoateHCID 6935607718%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 5-amino-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoate (D150) (650 mg, 2.6 mmol, 1 equiv) in a 48% aqueous HBr solution at 0° C. was added NaNO2 portionwise and the resulting mixture was stirred at 0° C. for 30 min. CuBr (260 mg, 1.82 mmol, 0.7 equiv) in a 48% aqueous HBr solution (1 ml) was added and the resulting mixture stirred at 90° C. for 1 h then cooled to room temperature and partitioned between H2O and AcOEt. The two layers were separated and the organic phase was dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (iso-hexane/AcOEt: 2/1) gave methyl 5-bromo-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoate (D156) (145 mg, 18%) as a white solid. [M+H]+=318.1, RT=2.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-07e59919ed414231a74392685effb30a
Source noteuspto-grants-2007_08