HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855974Generated: November 1, 2026
Hexane → alpha-(Cyclohexyl)-alpha,alpha-bis[2-(diisopropylamino)ethyl]acetamide
https://huagongshe.com/reaction/1855974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | alpha,alpha-Bis[2-(diisopropylamino)ethyl]-alpha-phenylacetamide | HCID 12612273 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Ruthenium dioxide | HCID 82848 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | alpha-(Cyclohexyl)-alpha,alpha-bis[2-(diisopropylamino)ethyl]acetamide | HCID 23347231 | — |
Reaction Steps
10 Parts of α,α-bis[2-(diisopropylamino)ethyl]-α-phenylacetamide is dissolved in 130 parts by volume of ethanol and the solution placed in pressure shaker with 1 part of ruthenium dioxide. Hydrogen is introduced at 1000 psi and the reaction mixture heated at about 125° C. and shaken for about 24 hours. Then, the reaction mixture is cooled to room temperature and filtered. The filtrate is stripped of solvent to give an oil. This oil is dissolved in methylene chloride, then hexane added to the solution, methylene chloride evaporated, and the hexane mixture cooled to give α-(cyclohexyl)-α,α-bis[2-(diisopropylamino)ethyl]acetamide, as a crystal solid melting at about 114°-115° C. This compound has the following structural formula ##STR49##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04217306 |
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| Source dataset | uspto-grants-1980_08 |
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| ORD ID | ord-123a16f7f1c3485f89dc95d12ea3e4ae |
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| Source note | uspto-grants-1980_08 |
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