HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252807Generated: October 30, 2026
Sodium hydride → Methyl 2-((bis(tert-butoxycarbonyl)amino)methyl)-5-fluorobenzoate
https://huagongshe.com/reaction/2252807
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Di-tert-butyl Iminodicarboxylate | HCID 279800 | — |
| Reactant | Methyl 2-(bromomethyl)-5-fluorobenzoate | HCID 15155455 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-((bis(tert-butoxycarbonyl)amino)methyl)-5-fluorobenzoate | HCID 58978006 | — |
Reaction Steps
In a dry flask under nitrogen, di-tert-butyl iminodicarboxylate (Aldrich, 3.86 g, 17.8 mmol) was dissolved in dry DMF (5 mL) and treated with NaH (60% dispersion in oil, 0.71 g, 17.8 mmol). After the evolution of gas had ceased, Methyl 2-(bromomethyl)-5-fluorobenzoate (4 g, 16.2 mmole) dissolved in DMF (5 mL) was added. An additional 5 mL of DMF was added to aid stirring. The reaction was stirred for 2 hrs, then partitioned between water and EtOAc. The organic layer was dried with Na2SO4, filtered and concentrated and the residue was purified on silica eluting first with toluene, then with a gradient of 0-5% MeOH(CHCl3. The impure product thus obtained was re-chromatographed on silica eluting with a gradient of 0-30% EtOAc/Hexanes. The product was obtained as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323460B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-54da8dd3562a4757b5d75d656b7142c3 |
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| Source note | uspto-grants-2008_01 |
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