Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexene oxide | HCID 9246 | — |
| Reactant | 1,4,7,10-Tetraazacyclododecane | HCID 64963 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86754875 | HCID 86754875 | — |
Reaction Steps
10 g (58.08 mmol) of 1,4,7,10-tetraazacyclododecane, 4.85 g (116.16 mmol) of LiCl and 56.5 g (580.0 mmol) of cyclohexene oxide (7-oxabicyclo[4.1.0]heptane) are suspended in 20 ml of isopropanol and refluxed for 20 hours. Then, the reaction mixture is mixed with 30 ml of isopropanol and slowly cooled to 0° C. The crystals that are obtained are suctioned off, washed with 30 ml of methyl-tert-butyl ether and dried in a vacuum. 19.5 g (82% of theory) of 1,7-bis(6-hydroxycyclohexyl)-1,4,7,10-tetraazacyclododecane LiCl complex is obtained as white crystals. Melting point 170-178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994536 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-75a0de9125ad415891ac44f8c1587374 |
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| Source note | uspto-grants-1999_11 |
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