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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDi-tert-butyl IminodicarboxylateHCID 279800—
ReactantMethyl 2-(bromomethyl)-5-fluorobenzoateHCID 15155455—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-((bis(tert-butoxycarbonyl)amino)methyl)-5-fluorobenzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323460B2
Source datasetuspto-grants-2008_01
ORD IDord-54da8dd3562a4757b5d75d656b7142c3
Source noteuspto-grants-2008_01