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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279440Generated: October 26, 2026

Hydrochloric Acid → alpha-Ethoxyimino-2-phenoxymethylbenzyl chloride

https://huagongshe.com/reaction/279440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantCarbon TetrachlorideHCID 5943—
Reactant1,1-DichloroethaneHCID 6365—
ReactantTriphenylphosphineHCID 11776—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(Phenoxymethyl)benzoic acidHCID 69761—
ReactantO-ethylhydroxylamine hydrochlorideHCID 76850—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Productalpha-Ethoxyimino-2-phenoxymethylbenzyl chlorideHCID 5454498193.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Dichloroethane (50 ml), thionyl chloride (6.54 g, 0.055 mol) and dimethylformamide (0.25 ml) were added to 2-phenoxymethylbenzoic acid (11.41 g, 0.05 mol), and the mixture was stirred at 80° C. for 2 hours. After completion of the reaction, the mixture was concentrated under reduced pressure, and the residue was dissolved in dichloromethane (25 ml). The solution was added to a mixture of ethoxyamine hydrochloride (5.85 g, 0.06 mol), pyridine (9.89 g, 0.125 mol) and dry dichloromethane (50 ml) under ice-cooling over 20 minutes, and then the resulting mixture was stirred at room temperature for 2 hours. After completion of the reaction, water (200 ml) was added, adjusted to pH<2 with conc. hydrochloric acid, and extracted with dichloromethane. The dichloromethane layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Acetonitrile (150 ml), triphenylphosphine (20.98 g, 0.08 mol) and carbon tetrachloride (24.61 g, 0.16 mol) were added to the residue, and the mixture was stirred under reflux for 1.5 hours. After completion of the reaction, the mixture was concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give α-ethoxyimino-2-phenoxymethylbenzyl chloride (13.51 g, 93.2%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362212B1
Source datasetuspto-grants-2002_03
ORD IDord-b427673e9dca4c3d9d10190d9e5ddcb3
Source noteuspto-grants-2002_03