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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050249Generated: October 30, 2026

Methanesulfonyl chloride → (4aR,7S,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl methanesulfonate

https://huagongshe.com/reaction/1050249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(4aR,7S,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-olHCID 58194975—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
Product(4aR,7S,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl methanesulfonateHCID 89051399—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (4aR,7S,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-ol (850 mg, 3.60 mmol) and DMAP (22 mg, 0.180 mmol) under nitrogen in anhydrous pyridine (10.0 mL) at 0° C. was added methanesulfonyl chloride (0.51 mL, 742 mg, 6.48 mmol) dropwise over 2 minutes. After stirring at 0° C. for 1.5 hours, the mixture was diluted with toluene (10 mL) and concentrated under reduced pressure. The resultant white solid was dissolved in DCM and filtered to remove solids. The filtrate was then chromatographed using a Biotage™ 50 g silica gel cartridge eluted with 0-50% EtOAc in 1:1 Hexane/DCM over 20 column volumes. The product fractions were combined and concentrated under reduced pressure to provide the title compound as a white solid. LC-MS: calculated for C14H18O6S 314.08, observed m/e: 315.06 (M+H)+ (Rt 1.56/4 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382243B2
Source datasetuspto-grants-2016_07
ORD IDord-88c28fe1343d4c299e0893e297e4165e
Source noteuspto-grants-2016_07