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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505642Generated: October 30, 2026

Azane;hydrate → (3R*,4S*)-4-amino-6-methoxy-2,2-dimethyl-7-nitro-3,4-dihydro-2H-1-benzopyran-3-ol

https://huagongshe.com/reaction/505642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzane;hydrateHCID 12896473—
Reactant(3R*,4R*)-3,4-epoxy-6-methoxy-2,2-dimethyl-7-nitro-3,4-dihydro-2H-1-benzopyranHCID 25196994—
SolventEthanolHCID 702—
Product(3R*,4S*)-4-amino-6-methoxy-2,2-dimethyl-7-nitro-3,4-dihydro-2H-1-benzopyran-3-olHCID 5903174984%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of (3R*,4R*)-3,4-epoxy-6-methoxy-2,2-dimethyl-7-nitro-3,4-dihydro-2H-1-benzopyran (2.64 g, 10.5 mmol) in ethanol (26 mL), an ammonia water (26 mL) was added, and the resulting mixture was stirred in a sealed tube at 100° C. for 2 hours. Upon the completion of the reaction, the solvent was distilled off. An aqueous solution of saturated sodium carbonate was added to the residue, and the resulting mixture was extracted with ethyl acetate. The organic phase was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and thereby the aimed product was obtained as red amorphous substance (yield: 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781483B2
Source datasetuspto-grants-2010_08
ORD IDord-0bb61f71ffe74a0184c35a136c2d5c84
Source noteuspto-grants-2010_08