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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716444Generated: November 3, 2026

4-Toluenesulfonyl chloride → (3R,3aS,6R,6aS)-6-[(4-methylbenzenesulfonyl)oxy]-hexahydrofuro[3,2-b]furan-3-yl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/1716444

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPotassium HydroxideHCID 14797—
Reactant1,4:3,6-Dianhydro-D-mannitolHCID 10975624—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Product(3R,3aS,6R,6aS)-6-[(4-methylbenzenesulfonyl)oxy]-hexahydrofuro[3,2-b]furan-3-yl 4-methylbenzene-1-sulfonateHCID 5103320048.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Isomannide (40) (50 g, 342.5 mmol) and p-toluenesulphonyl chloride (143.6 g, 753.2 mmol) were dissolved in a mixture of carbon tetrachloride (300 mL), dichloromethane (30 mL) and water (250 mL). The flask was cooled to 0° C. and a solution of potassium hydroxide (42.0 g, 750.0 mmol) in water (42 mL) added dropwise over 2 hours with stirring under argon. The resulting biphasic mixture was stirred vigorously at 0° C. for 24 hours. The resulting off-white precipitate, comprising a mixture of mono- and bistosylates (approximately 1:1), was collected by filtration in vacuo. The filter cake was washed with water then triturated with methanol (500 mL). The solid was isolated by filtration in vacuo to obtain ditosylate (39) as an off-white powder (75 g, 48%). [□]D18+96.7° (c=10.5, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803803B2
Source datasetuspto-grants-2010_09
ORD IDord-387ee0b095184155a8ad172f74136fd6
Source noteuspto-grants-2010_09