HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172452Generated: October 27, 2026
Dimethylformamide → Tert-butyl 4-(2-fluoro-3-formylbenzoyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1172452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylate | HCID 57562603 | — |
| Reactant | HCID 178418368 | HCID 178418368 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(2-fluoro-3-formylbenzoyl)piperazine-1-carboxylate | HCID 57562639 | — |
Reaction Steps
194 mg of tert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylate was dissolved in 5.0 ml of tetrahydrofuran, and 1.25 ml of a solution of isobutyl magnesium chloride in tetrahydrofuran (2.0 M) was added thereto at −78° C. After stirring at the same temperature for 2 hours, 0.39 ml (5.0 mmol) of N,N-dimethylformamide was added thereto. The resulting mixture was stirred at the same temperature for 30 minutes and further stirred at 0° C. for 30 minutes. To the reaction mixture was added saturated ammonium chloride, and the mixture was extracted with chloroform. The organic layer was washed with brine and then concentrated. The residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate=9/1 to 1/1) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834018B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-8101c7d7376a4209950002c7019f1b76 |
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| Source note | uspto-grants-2010_11 |
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