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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423179Generated: October 25, 2026

1-Butyne → 1-But-1-ynyl-4-fluoro-2-methoxymethoxy-benzene

https://huagongshe.com/reaction/423179

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButyneHCID 7846—
Reactant1-Bromo-4-fluoro-2-(methoxymethoxy)benzeneHCID 10823625—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiethyl EtherHCID 3283—
SolventDiethylamineHCID 8021—
Product1-But-1-ynyl-4-fluoro-2-methoxymethoxy-benzeneHCID 5956517691%

Reaction Conditions

Temperature70 °C

Reaction Steps

1-Bromo-4-fluoro-2-methoxymethoxy-benzene (7.6 g, 32 mmol) is placed in a pressure flask, dissolved in diethylamine (65 mL) and degassed with nitrogen for 15 min. An excess of butyne is bubbled through the solution, CuI (1.9 g, 10 mmol) and PdCl2(PPh3)2 (2.3 g, 3.3 mmol) are added, and the flask is heated to 70° C. for 44 h. The mixture is diluted with ether, then washed with saturated aqueous NH4Cl and brine. The organic portion is dried over MgSO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (Biotage® Si65M, 3% THF/hexane) to provide 6.12 g (91%) of the title compound as an orange solid. GCMS m/e 208 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101761B2
Source datasetuspto-grants-2012_01
ORD IDord-bc3a652c23944c49801cf9ef32298cc6
Source noteuspto-grants-2012_01