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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63851Generated: November 1, 2026

Dichloromethane → HCID 118046905, compound

https://huagongshe.com/reaction/63851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 86654468HCID 86654468—
Reactant(NE)-N-[[4-bromo-3-(trifluoromethyl)phenyl]methylidene]hydroxylamineHCID 118046913—
SolventWaterHCID 962—
ProductHCID 118046905HCID 118046905—

Reaction Steps

Into a 50-mL round-bottom flask, was placed (E)-N-[[4-bromo-3-(trifluoromethyl)phenyl]methylidene]hydroxylamine (1.5 g, 5.60 mmol, 1.00 equiv), dichloromethane (20 mL), 1-chloro-3-(trifluoromethyl)-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene (1.6 g, 5.83 mmol, 1.10 equiv), NaOCl (10 mL). The resulting solution was stirred for 2 h at room temperature. The resulting solution was diluted with 30 mL of H2O. The resulting solution was extracted with 3×50 mL of dichloromethane and the organic layers combined. The resulting mixture was washed with 3×50 mL of brine. The mixture was dried over anhydrous sodium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:100). This resulted in 1.7 g (56%) of 3-[4-bromo-3-(trifluoromethyl)phenyl]-5-[3-chloro-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-4,5-dihydro-1,2-oxazole as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447084B2
Source datasetuspto-grants-2016_09
ORD IDord-a7ba6a442adc43b2bbeb94ef9c884f1a
Source noteuspto-grants-2016_09