HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946684Generated: October 26, 2026
Cyclohexanone → N-(2-methoxyethyl)cyclohexanamine
https://huagongshe.com/reaction/1946684
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2-methoxyethyl)cyclohexanamine | HCID 12687399 | — |
Reaction Steps
A solution of cyclohexanone (10 g, 0.10 mol) in Toluene (100 ml) was treated with 2-methoxy ethylamine (8.4 g, 0.11 mol) and refluxed at 110° C. for 3 h. The reaction mass was cooled and diluted with ethanol (50 ml) and sodium borohydride (5.8 g, 0.15 mol) was added in portions at 0° C. The reaction mass was stirred at RT for 12 h and concentrated under reduced pressure. The residue was dissolved in water (100 ml), extracted with DCM (2×100 ml), dried over sodium sulphate and evaporated. The crude material was purified by column chromatography by using DCM and methanol (98:2) as eluent to afford the title compound as a pale yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399448B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-10dffc8a62a34bbc906762cd50b4de6e |
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| Source note | uspto-grants-2013_03 |
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