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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215960Generated: October 26, 2026

Ethylene Glycol → HCID 178517865, compound

https://huagongshe.com/reaction/215960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Bromo-1-fluoro-2-iodobenzeneHCID 2782750—
ReactantHCID 178517868HCID 178517868—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
ProductHCID 178517865HCID 17851786570%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-(cis-4-hydroxycyclohexyl)-2,8-diazaspiro[4.5]decan-1-one (0.50 g, 2.0 mmol), 4-bromo-1-fluoro-2-iodobenzene (0.894 g, 2.97 mmol), copper(I) iodide (0.0586 g, 0.308 mmol), potassium phosphate (1.26 g, 0.596 mmol) and 1,2-ethanediol (0.23 mL, 4.1 mmol) in 1-butanol (2.5 mL) was heated at 100° C. overnight. The reaction mixture was treated with water, extracted with ether. The combined organic layers were washed with brine, dried over MgSO4 and filtered. The filtrate was concentrated under reduced pressure. The residue was purified on a silica gel column with ethyl acetate in hexane (gradient: 0 to 50%) to give the desired product (0.59 g, 70%). LCMS: (M+H)+=425.0/427.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193207B2
Source datasetuspto-grants-2012_06
ORD IDord-d50c91e1934e43d382c73f612ede010c
Source noteuspto-grants-2012_06