HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909873Generated: November 2, 2026
Cyclohexylamine → N-(2,2-dimethoxyethyl)cyclohexanamine
https://huagongshe.com/reaction/909873
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-1,1-dimethoxyethane | HCID 60986 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2,2-dimethoxyethyl)cyclohexanamine | HCID 3024915 | — |
Reaction Steps
2-Chloro-1,1-dimethoxyethane (206 mL) was treated with cyclohexanamine (575 mL) and the mixture was heated at 120° C. for 24 h under an atmosphere of nitrogen before being cooled to room temperature. A solution of sodium hydroxide (100 g) in 400 mL water was added, the mixture was stirred at room temperature for 10 min and then the layers were separated. The organic fraction was purified by distillation under reduced pressure (b.p. 105-107° C., 13 mm Hg) to give the title compound as a colourless oil (280 g). 1H NMR (400 MHz, CDCl3) δ 4.46 (t, J=5.5 Hz, 1H), 3.38 (s, 6H), 2.75 (d, J=5.6 Hz, 2H), 2.45-2.35 (m, 1H), 1.92-1.57 (m, 5H), 1.31-1.00 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017602B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-1933f7889c5742e69ef6250271630ccc |
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| Source note | uspto-grants-2011_09 |
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