HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505644Generated: October 30, 2026
Ammonium Chloride → HCID 59031753, compound
https://huagongshe.com/reaction/505644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium perchlorate | HCID 23665649 | — |
| Reactant | HCID 59031741 | HCID 59031741 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59031753 | HCID 59031753 | 99% |
Reaction Steps
To a solution of (3R*,4R*)-3,4-epoxy-2,2,8-trimethyl-7-nitro-3,4-dihydro-2H-1-benzopyran (600 mg, 2.55 mmol) in 1,4-dioxane (1.2 mL), lithium perchlorate (271 mg, 2.55 mmol) and 2-(phenylethyl)amine (0.384 mL, 3.06 mmol) were added at room temperature and the mixture was stirred at 80° C. for 1 hour. Upon the completion of the reaction, saturated ammonium chloride was added to the reaction solution, and the resulting solution was extracted with ethyl acetate. The organic phase was washed with saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. After distilling off the solvent, the residue was purified by column chromatography (hexane/ethyl acetate=4/1) and the aimed product was obtained as orange oily substance (yield: 99%).
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-6becf64cec2348cf86202c77d7245a7d |
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| Source note | uspto-grants-2010_08 |
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