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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414645Generated: October 30, 2026

Diethyl Ether → HCID 14424685, compound

https://huagongshe.com/reaction/414645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-4'-fluoroacetophenoneHCID 120248—
ReactantHCID 178418486HCID 178418486—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14424685HCID 1442468566%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 0.12 mol of ethynylmagnesium bromide in 300 mL of dry THF at 23° C. was added 15.5 g (90 mmol) of 2-chloro-4'-fluoro-acetophenone as a solid. The mixture stirred at 23° C. for 24 hours when it was quenched with 15 mL of saturated NH4Cl and poured int 250 mL of diethyl ether. The ether layer was separated and washed with H2O, dried (MgSO4) and concentrated. The residue was added to 300 mL of dry diethyl ether and 3.6 g (90 mmol) of pulverized NaOH was added. The reaction mixture was stirred at 23° C. for 3 hours, then the ether was washed twice with 100 mL of H2O and once with saturated brine. The organic layer was dried (MgSO4), concentrated and distillation (b.p. 55°-58° C. at 0.34 mmHg) provided 9.5 g (66%) of 3,4-epoxy- 3-(4'-fluorophenyl)-1-butyne as a liquid, homogeneous by spectroscopic criteria; IR (film) 3275, 1595, 1505, 1218 cm-1 ; 1HNMR (80 MHz, CDCl3) δ 7.45 (m, 2H), 7.15 (m, 2H), 3.20 (ABq, 2H, J=8.0 Hz, ΔνAB =39.2 Hz), 2.51 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792614
Source datasetuspto-grants-1988_12
ORD IDord-e9334638a62c4c89ab9d70a09edeb036
Source noteuspto-grants-1988_12