HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205982Generated: November 1, 2026
Diisopropyl Ether → 4-Benzyl-2-methoxypyridin-3-amine
https://huagongshe.com/reaction/2205982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Tert-butyl (4-benzyl-2-methoxypyridin-3-yl)carbamate | HCID 10245115 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Benzyl-2-methoxypyridin-3-amine | HCID 117987838 | 50.8% |
Reaction Steps
To a solution of tert-butyl (4-benzyl-2-methoxypyridin-3-yl)carbamate (25.4 g) in ethyl acetate (202 mL) was added 4N hydrogen chloride/ethyl acetate solution (202 mL) at room temperature, and the mixture was stirred overnight at room temperature, and then at 50° C. for 1 hr. To the reaction mixture was added diisopropyl ether at room temperature, and the obtained precipitate was collected by filtration, and washed with diisopropyl ether. Saturated aqueous sodium hydrogencarbonate solution was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (basic silica gel, ethyl acetate/hexane) to give the title compound (8.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371320B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-4e05ceae2f584ab799142f2ef9fe2878 |
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| Source note | uspto-grants-2016_06 |
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