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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (NE)-N-[(4-bromo-3-methylphenyl)methylidene]hydroxylamine | HCID 21833735 | — |
| Reactant | 1,3-Dichloro-2-fluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene | HCID 58468233 | — |
| Reactant | HCID 178521654 | HCID 178521654 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118046969 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447084B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-49d98bb8092f4964a6da6d10735e8f9b |
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| Source note | uspto-grants-2016_09 |
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