HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108949Generated: October 29, 2026
1,2-Dichlorobenzene → HCID 18995918, compound
https://huagongshe.com/reaction/1108949
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | 4-((3-Chloro-5-(trifluoromethyl)pyridin-2-yl)oxy)benzonitrile | HCID 2744478 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | N-methyl-N-phenylsulfonyl-2-chloro-6-fluorobenzohydrazonoyl chloride | HCID 53760501 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 18995918 | HCID 18995918 | 43.3% |
Reaction Steps
A mixture of 1.30 g of N-methyl-N-phenylsulfonyl-2-chloro-6-fluorobenzohydrazonoyl chloride, 1.00 g of 4-(3-chloro-5-trifluoromethylpyridin-2-yloxy)benzonitrile, 0.50 g of anhydrous aluminum chloride and 3 ml of o-dichlorobenzene was stirred in an oil bath at a temperature of 140° C. for 30 minutes. After the cooling, the resulting solution was dissolved in 100 ml of chloroform, washed with diluted hydrochloric acid solution, diluted sodium hydroxide solution and saline water in this order, dried over anhydrous magnesium sulfate and concentrated under a reduced pressure. The resulting concentrate was purified through a chromatography of silica gel column using a mixed solution of hexane and ethyl acetate as a developing solvent to obtain 0.70 g of the given compound (measurement of nD20 was impossible). NMR data (60 MHz, CDCl3 solvent, δ value)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05318959 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-1e2f31687c2645138810dce7cd8864bc |
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| Source note | uspto-grants-1994_06 |
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