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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | Methyl 5-amino-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoate | HCID 69357536 | — |
| Product | Methyl 5-bromo-2-fluoro-3-(2-oxo-1-pyrrolidinyl)benzoate | HCID 69356077 | 18% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253198B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-07e59919ed414231a74392685effb30a |
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| Source note | uspto-grants-2007_08 |
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