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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | (3R*,4R*)-3,4-epoxy-6-methoxy-2,2-dimethyl-7-nitro-3,4-dihydro-2H-1-benzopyran | HCID 25196994 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3R*,4S*)-4-amino-6-methoxy-2,2-dimethyl-7-nitro-3,4-dihydro-2H-1-benzopyran-3-ol | HCID 59031749 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781483B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-0bb61f71ffe74a0184c35a136c2d5c84 |
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| Source note | uspto-grants-2010_08 |
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