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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495526Generated: October 31, 2026

Methoxymethyl-triphenylphosphonium chloride → HCID 69615387, compound

https://huagongshe.com/reaction/495526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant1-(2,6-Difluorobenzyl)-2,6-dimethyl-3-bromo-5-formyl-4-pyridoneHCID 22327225—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69615387HCID 69615387—

Reaction Conditions

Temperature-78 °C

Reaction Steps

KHMDS (2.4 mmol, 4.8 mL of a 0.5 M solution in toluene) was added dropwise to a vigorously stirred suspension of (methoxymethyl)triphenylphosphonium chloride (771 mg, 2.25 mmol) in anhydrous THF (8 mL), at −78° C. under N2. The resulting orange suspension was stirred at −78° C. for 45 min. Then, a solution of 1-(2,6-difluorobenzyl)-2,6-dimethyl-3-bromo-5-formyl-4-pyridone (534 mg, 1.50 mmol) in THF (8 mL) was added dropwise and the reaction was allowed to warm slowly to room temperature. After 1 h at room temperature, the reaction was quenched with an aqueous saturated solution of NaHCO3. The organics were extracted with EtOAc (50 mL), the organic layer was separated, washed with H2O and brine, dried over MgSO4, filtered and evaporated under vacuum. The crude residue was utilized in the next step. LRMS m/z 384.0 (M+−1), 386.0 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939883B2
Source datasetuspto-grants-2005_09
ORD IDord-900fce02e0ea45feb6eca1a3c19477d6
Source noteuspto-grants-2005_09