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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387367Generated: October 29, 2026

Dichloromethane → HCID 3441033, compound

https://huagongshe.com/reaction/1387367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethyl (methoxyimino)(2-{[({1-[3-(trifluoromethyl)phenyl]ethylidene}amino)oxy]methyl}phenyl)acetateHCID 213016—
ReactantDiisobutylaluminumhydride tolueneHCID 86583787—
SolventMethanolHCID 887—
ProductHCID 3441033HCID 3441033109.6%

Reaction Steps

1M diisobutylaluminum hydride/toluene solution (11 ml, 16.5 mmol) was added dropwise to a mixture of methyl 2-[(α-methyl-3-trifluoromethylbenzylidene)aminooxymethyl]-α-methoxyiminophenylacetate (4.83 g, 11.8 mmol) and dichloromethane (47 ml) at −65° C. or lower over 4 minutes, and the mixture was stirred at −78° C. to room temperature for 3 hours. Methanol (7 ml) was added to the reaction mixture, and the mixture was stirred at room temperature for 1 hour. The precipitated insoluble materials were removed, and the remaining mixture was concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give 2-[(α-methyl-3-trifluoromethylbenzylidene)aminooxymethyl]-(α-methoxyiminophenylacetaldehyde (2.11 g, 47.3%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268312B1
Source datasetuspto-grants-2001_07
ORD IDord-6510a90b7cb8415bb41757fbc291ce42
Source noteuspto-grants-2001_07