HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642962Generated: October 27, 2026
Water → N-Methyl-N-{2-[(tributylstannyl)methoxy]ethyl}cyclohexaneamine
https://huagongshe.com/reaction/642962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Cyclohexylmethylamino)ethanol | HCID 277582 | — |
| Reactant | Tributyl(iodomethyl)stannane | HCID 10862926 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Methyl-N-{2-[(tributylstannyl)methoxy]ethyl}cyclohexaneamine | HCID 59259719 | 86% |
Reaction Steps
To a mixture of sodium hydride (50%, 241 mg, 5.0 mmol) and tetrahydrofuran (20 ml) was added 2-[cyclohexyl(methyl)amino]ethanol (791 mg, 5.0 mmol) at 0° C. (external temperature). Then, the reaction mixture was stirred at 60° C. for 30 minutes. After the reaction mixture was cooled at 0° C. (external temperature), to the reaction mixture was added dropwise a solution of tributyl-iodomethyl-tin (2.2 g, 5.0 mmol) in tetrahydrofuran (5 ml), and the reaction mixture was stirred at 60° C. for 1 hour. After the reaction mixture was cooled at room temperature (external temperature), water was added to stop the reaction. Ethyl acetate was added to the reaction mixture, and the organic layer was separated. After the organic layer was washed with water, an aqueous saturated sodium chloride solution, and then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (heptane:ethyl acetate=20:1, NH silica gel) to obtain the title compound (790.7 mg, 4.3 mmol, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07696347B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-210dbaacbcd64b4dbdd1bdd888419e6a |
|---|
| Source note | uspto-grants-2010_04 |
|---|