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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217971Generated: October 30, 2026

(+/-)-(3aR*,7aS*)-7a-(2-fluorophenyl)hexahydropyrano[3,4-c]isoxazole → (+/-)-[(3S*,4R*)-3-amino-3-(2-fluorophenyl)tetrahydropyran-4-yl]methanol

https://huagongshe.com/reaction/217971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-(3aR*,7aS*)-7a-(2-fluorophenyl)hexahydropyrano[3,4-c]isoxazoleHCID 59281199—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product(+/-)-[(3S*,4R*)-3-amino-3-(2-fluorophenyl)tetrahydropyran-4-yl]methanolHCID 5840605286.6%

Reaction Steps

Zinc (11.6 g) was added to a solution of (±)-(3aR*,7aS*)-7a-(2-fluorophenyl)hexahydropyrano[3,4-c]isoxazole (3.95 g) in acetic acid (78.4 ml), and the mixture was stirred at room temperature overnight. The insoluble matter was removed by filtration through celite, and the solvent was evaporated under reduced pressure. An ice-cooled 0.5 N sodium hydroxide solution was added to the residue. The aqueous layer was extracted with ethyl acetate and a mixed solution of ethyl acetate and tetrahydrofuran. The organic layers were combined and washed with brine and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to obtain the title compound (3.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198269B2
Source datasetuspto-grants-2012_06
ORD IDord-dde860a2e3604669847f57b8dfb9ae5f
Source noteuspto-grants-2012_06