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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63877Generated: October 30, 2026

(NE)-N-[(4-bromo-3-methylphenyl)methylidene]hydroxylamine → HCID 118046969, compound

https://huagongshe.com/reaction/63877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(NE)-N-[(4-bromo-3-methylphenyl)methylidene]hydroxylamineHCID 21833735—
Reactant1,3-Dichloro-2-fluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzeneHCID 58468233—
ReactantHCID 178521654HCID 178521654—
SolventDichloromethaneHCID 6344—
ProductHCID 118046969HCID 118046969—

Reaction Steps

Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed dichloromethane (10 mL), (E)-N-[(4-bromo-3-methylphenyl)methylidene]hydroxylamine (50 mg, 0.23 mmol, 1.00 equiv), 1,3-dichloro-2-fluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene (60 mg, 0.23 mmol, 1.00 equiv), chlorosylsodium (5 mL). The resulting solution was stirred overnight at room temperature. The resulting solution was diluted with 50 mL of DCM. The resulting mixture was washed with 3×10 mL of brine. The organic phase was dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 82 mg (75%) of 3-(4-bromo-3-methylphenyl)-5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydro-1,2-oxazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447084B2
Source datasetuspto-grants-2016_09
ORD IDord-49d98bb8092f4964a6da6d10735e8f9b
Source noteuspto-grants-2016_09