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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433799Generated: October 30, 2026

Ethylene Glycol → HCID 68618823, compound

https://huagongshe.com/reaction/1433799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantAzetidineHCID 10422—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
CatalystCopper iodideHCID 83717—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
ProductHCID 68618823HCID 6861882381%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-fluoro-4-iodoaniline (1 g, 4.14 mmol), copper iodide (304 mg, 0.21 mmol) and potassium phosphate (1.75 g, 8.27 mmol) in ethylene glycol (465 μl, 8.27 mmol) and isopropanol (4 mL) in a bomb flask was added azetidine (304 mg, 5.17 mmol). The flask was sealed and heated to 80° C. for 24 hours. The reaction mixture was dissolved in ethyl acetate (50 mL), washed with water (3×50 mL), brine (50 mL), and the brine layer back extracted with ethyl acetate (2×50 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo to a brown oil. The oil was purified by chromatography over silica gel eluted with 40% v/v ethyl acetate in hexanes. The product containing fractions were combined and concentrated to give 4-azetidin-1-yl-2-fluoro-phenylamine as an orange oil (555 mg, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612212B2
Source datasetuspto-grants-2009_11
ORD IDord-9872ef8f04314c79be82978671bae91b
Source noteuspto-grants-2009_11