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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604710Generated: November 2, 2026

Cyclohexene oxide → HCID 86754875, compound

https://huagongshe.com/reaction/1604710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexene oxideHCID 9246—
Reactant1,4,7,10-TetraazacyclododecaneHCID 64963—
ReactantLithium ChlorideHCID 433294—
SolventIsopropanolHCID 3776—
ProductHCID 86754875HCID 86754875—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994536
Source datasetuspto-grants-1999_11
ORD IDord-75a0de9125ad415891ac44f8c1587374
Source noteuspto-grants-1999_11