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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050250Generated: November 2, 2026

Sodium Azide → (4aR,7R,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-amine

https://huagongshe.com/reaction/1050250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantAzideHCID 33558—
ReactantTrimethylphosphineHCID 68983—
Reactant(4aR,7S,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl methanesulfonateHCID 89051399—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product(4aR,7R,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-amineHCID 90044786—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of (4aR,7S,8aS)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl methanesulfonate (109 mg, 0.347 mmol) under nitrogen in anhydrous DMF (2.0 mL) was added sodium azide (90 mg, 1.387 mmol). The mixture was heated to 80° C. After 24 hours, the mixture was concentrated under reduced pressure. The resultant oil was chromatographed using a Biotage™ 10 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. The resultant white solid (67 mg, 0.256 mmol) was dissolved in anhydrous THF (2.0 mL) under nitrogen and a IM solution of trimethylphosphine (0.51 mL, 0.51 mmol) was added. The mixture was allowed to stir at room temperature for 40 minutes until the azide was consumed, then saturated aqueous ammonium hydroxide (0.5 mL) was added. After stirring for 30 minutes, the mixture was concentrated under reduced pressure and dried under high vacuum. The resultant residue was dissolved in acetonitrile (2 mL), frozen at −78° C., and lyophilized to dryness to provide the title compound as a white solid. LC-MS: calculated for C13H17NO3 235.12, observed m/e: 236.19 (M+H)+ (Rt 0.45/4 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382243B2
Source datasetuspto-grants-2016_07
ORD IDord-5efecd7da7ff441fbf13123b2d250a38
Source noteuspto-grants-2016_07