Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095900Generated: October 25, 2026

Hydrochloric Acid → 4-[3-Chloro-4-(1-methyl-2-oxo-ethyl)-phenoxy]-benzonitrile

https://huagongshe.com/reaction/1095900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(4-Acetyl-3-chlorophenoxy)benzonitrileHCID 64335501—
SolventTetrahydrofuranHCID 8028—
Product4-[3-Chloro-4-(1-methyl-2-oxo-ethyl)-phenoxy]-benzonitrileHCID 86645948—

Reaction Steps

Potassium tert-butoxide (248 mg) was added to a solution 4-(4-acetyl-3-chloro-phenoxy)-benzonitrile (500 mg) and (methoxymethyl)-triphenylphosphonium chloride (694 mg) in THF (10 ml) at room temperature. The mixture was stirred for 1 h at room temperature. 25% aqueous HCl (4 ml) was added. The resulting mixture was stirred 1 h at room temperature and poured then carefully to a saturated aqueous NaHCO3 solution. After neutralization, the mixture was extracted with EtOAc. The combined organic layers were dried over Na2SO4 and then concentrated to an oil. The residue was purified by flash chromatography (SiO2, EtOAc/heptane 1:2) to give the title compound (450 mg) as yellow oil. MS (m/e, ISP neg. ion)=284.3 [M−H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138189B2
Source datasetuspto-grants-2012_03
ORD IDord-e8ddd91e87ed4d8bb16d6688a903ae58
Source noteuspto-grants-2012_03