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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(Phenoxymethyl)benzoic acid | HCID 69761 | — |
| Reactant | O-ethylhydroxylamine hydrochloride | HCID 76850 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | alpha-Ethoxyimino-2-phenoxymethylbenzyl chloride | HCID 54544981 | 93.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06362212B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-b427673e9dca4c3d9d10190d9e5ddcb3 |
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| Source note | uspto-grants-2002_03 |
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