Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072887Generated: October 30, 2026

Sodium Iodide → 1-Phthalimido-4-p-toluenesulfonyl-6,6-difluoro-8-benzyloxy-4-aza-octane

https://huagongshe.com/reaction/2072887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantN-3-BromopropylphthalimideHCID 21611—
ReactantN-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamideHCID 19860703—
ReactantPotassium tertbutoxideHCID 50987170—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product1-Phthalimido-4-p-toluenesulfonyl-6,6-difluoro-8-benzyloxy-4-aza-octaneHCID 19860707—

Reaction Steps

To a solution of N-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamide (7.0 g, 19 mM) in dry DMF (20 mL), is added potassium-tert.-butoxide (2.34 g, 21 mmoles), and the mixture is stirred for 30 minutes. To this mixture are added N-3-bromopropyl-phthalimide (5.1 g, 19 mmoles) and sodium iodide (0.33 g), and the entire mixture is then stirred overnight under nitrogen at room temperature. Following the addition of brine, the mixture is extracted with ether, washed with 1N HCl (twice), then with brine (twice), and dried over Na2SO4. Evaporation of the solvent yields 1-phthalimido-4-p-toluenesulfonyl-6,6-difluoro-8-benzyloxy-4-aza-octane as an oil, which crystallizes on scratching with ether/petroleum ether to form white crytals: 9.5 g (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914240
Source datasetuspto-grants-1990_04
ORD IDord-2fc3db3ba2e443a4a4d1dca979f34f88
Source noteuspto-grants-1990_04