HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533888Generated: October 30, 2026
Triethylamine → 3-(4-Bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole
https://huagongshe.com/reaction/533888
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 1,3-Dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene | HCID 23159823 | — |
| Reactant | 4-Bromo-3-methylbenzaldehyde oxime | HCID 73847954 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole | HCID 23159812 | 54.1% |
Reaction Steps
To a solution of 4-Bromo-3-methyl-benzaldehyde oxime (2.600 g, 12.15 mmol) in DMF (40 mL) was added N-chloro succinimide (1.700 g, 12.73 mmol) and the mixture was heated at 70° C. (bath temperature) for 1 h. After cooling to 0° C., a solution of 1,3-dichloro-5-(1-trifluoromethyl-vinyl)-benzene (2.900 g, 12.03 mmol) in DMF (8 mL), followed by triethylamine (2.00 g, 2.75 mL, 19.8 mmol) was added. After 1 h at this temperature, the cooling bath was removed and the mixture was stirred over night. The mixture was separated between MTBE and aqueous NH4Cl solution. The organic layer was separated and the solvent was removed in vacuum. Column chromatography on SiO2 with heptane/CH2Cl2 gave the title compound (2.95 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853410B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-399910df2b6246f6a77364be8dd8a77b |
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| Source note | uspto-grants-2014_10 |
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