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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232167Generated: October 30, 2026

Pyridine → 1-Phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-methanesulfonyloxy-4-aza-octane

https://huagongshe.com/reaction/232167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-hydroxy-4-aza-octaneHCID 13935585—
ReactantAcetone cyclohexaneHCID 21916603—
SolventDichloromethaneHCID 6344—
Product1-Phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-methanesulfonyloxy-4-aza-octaneHCID 13935586—

Reaction Steps

To a solution of 1-phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-hydroxy-4-aza-octane (56.0 g, 120 mmoles) and dry pyridine (50 mL) in dry dichloromethane (400 mL), a solution of methanesulfonylchloride (14.4 g, 1.05 equivalents) in dichloromethane is added slowly at room temperature. After stirring overnight at room temperature, the mixture is washed with 1N HCl (500 mL), 10% aqueous NaHSO3 (250 mL), and water (250 mL). Drying (Na2SO4) and evaporation of the solvent yields an oil which solidifies under oil pump vacuum. Digestion with an acetone/cyclohexane mixture gives colorless crystals of 1-phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-methanesulfonyloxy-4-aza-octane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851448
Source datasetuspto-grants-1989_07
ORD IDord-292c7899093f4b8e918ff45b63924d8d
Source noteuspto-grants-1989_07