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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205646Generated: October 31, 2026

Ethylene Glycol → HCID 178517853, compound

https://huagongshe.com/reaction/2205646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Bromo-2-fluoro-1-iodobenzeneHCID 2724516—
ReactantHCID 178517863HCID 178517863—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1-ButanolHCID 263—
ProductHCID 178517853HCID 17851785354.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (5S)-2-(cis-4-hydroxycyclohexyl)-2,7-diazaspiro[4.5]decan-1-one (1.04 g, 0.00412 mol), 4-bromo-2-fluoro-1-iodobenzene (Aldrich, cat #: 283304) (1.85 g, 0.00615 mol), copper(I) iodide (Aldrich, cat #: 215554) (0.122 g, 0.000640 mol), potassium phosphate (2.63 g, 0.0124 mol) and 1,2-ethanediol (0.48 mL, 0.0086 mol) in 1-butanol (3.90 mL) was heated at 100° C. under nitrogen for 2 d. The reaction was quenched with water, and extracted with ether. The organic layers were combined, washed with water, brine, dried over Na2SO4, and filtered. The filtrate was evaporated under reduced pressure. The residue was purified by flash column chromatography on a silica gel column eluting with 0 to 5% methanol in DCM to yield the desired product (950 mg, 54.2%). LC/MS m/e 425.1/427.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371323B2
Source datasetuspto-grants-2016_06
ORD IDord-29fac59f7124407bbdb6383b02d7babb
Source noteuspto-grants-2016_06