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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355447Generated: October 30, 2026

Sodium Iodide → Diethyl 2-acetamido-2-((3,3-difluorocyclobutyl)methyl)malonate

https://huagongshe.com/reaction/2355447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetamidomalonic acid diethyl esterHCID 14041—
ReactantSodium hydrideHCID 24758—
ReactantIodide IonHCID 30165—
Reactant4-BromobenzenesulfonateHCID 1551619—
ReactantHCID 59382908HCID 59382908—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-acetamido-2-((3,3-difluorocyclobutyl)methyl)malonateHCID 67189917—

Reaction Conditions

Temperature0 °C

Reaction Steps

(3,3-Difluorocyclobutyl)methyl 4-bromobenzenesulfonate (500 mg, 1.47 mmol) and NaI (220 mg, 1.47 mmol, 1.0 equiv) were stirred in dry DMF (4 mL). In a separate 3-neck, 100 mL flask NaH (60 wt % in oil, 352 mg, 8.82 mmol, 6 equiv) was slurried in dry DMF (20 mL). The flask was cooled to 0° C. and diethyl-2-acetamidomalonate was added via syringe. After gas evolution ceased, the solution of the (3,3-difluorocyclobutyl)methyl 4-bromobenzenesulfonate and NaI In DMF was added. The resulting solution was heated to 45° C. for 17 h. After this time no remaining brosylate or iodide was observed by TLC and LC-MS. The mixture was quenched by dropwise addition of water (10 mL) and the DMF was removed in vacuo. The residue was partitioned between ether and water and the layers separated. The aqueous layer was extracted with additional ether and the combined organic layers were washed with brine. The residue was evaporated and the desired product was purified by flash chromatography on silica, eluting with 0 to 50% EtOAc in hexanes. The fractions were stained with ceric ammonium molybdate; the desired product is contained in the second spot. This afforded diethyl 2-acetamido-2-((3,3-difluorocyclobutyl)methyl)malonate (474 mg, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-2b8bb72bbe894dc29562c4c3c0a251c9
Source noteuspto-grants-2010_07