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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616866Generated: November 2, 2026

Ethylene Glycol → HCID 67324889, compound

https://huagongshe.com/reaction/1616866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantDimethylformamideHCID 6228—
Reactantm-FluorobenzenethiolHCID 75710—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 67324040HCID 67324040—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
ProductHCID 67324889HCID 67324889—

Reaction Conditions

Temperature120 °C

Reaction Steps

To tert-butyl 7-iodo-1,1-dimethyl-3,4-dihydro[1]benzofuro[2,3-c]pyridine-2(1H)-carboxylate P30 (0.505 g, 1.18 mmol) was added sodium tert-butoxide (341 mg, 3.55 mmol), copper(I) iodide (20 mg, 0.08 mmol), 1,2-ethanediol (132 μL, 2.38 mmol), N,N-dimethylformamide (17 mL, 210 mmol), and finally 3-Fluoro-benzenethiol (101 μL, 1.19 mmol). The reaction mixture was flushed with N2 and heated at 120° C. under N2. After 15 h, the reaction mixture was concentrated under high vacuum, the residue dissolved in 5% methanol-methylene chloride and then filtered through a celite-silica plug. The filtrate was concentrated and purified by silica chromatography (EtOAc/hexane) to afford the product as a pale yellow oil. MS m/z: 428 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765779B2
Source datasetuspto-grants-2014_07
ORD IDord-5e983adcc6684dbc9df917dc8068f941
Source noteuspto-grants-2014_07