HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52216Generated: October 28, 2026
1,2-Dichlorobenzene → 5-(4-chloro-3-octyloxyphenyl)-3-(2-chlorophenyl) 1-methyl-1H-1,2,4-triazole
https://huagongshe.com/reaction/52216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | 4-Chloro-3-octyloxybenzonitrile | HCID 21463669 | — |
| Reactant | N-methyl-N-phenylsulfonyl-2-chlorobenzohydrazonoyl chloride | HCID 54508988 | — |
| Catalyst | Iron chloride (FeCl3) | HCID 24380 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-(4-chloro-3-octyloxyphenyl)-3-(2-chlorophenyl) 1-methyl-1H-1,2,4-triazole | HCID 21463632 | 42.3% |
Reaction Steps
A mixture of N-methyl-N-(benzenesulfonyl)-2-chlorobenzohydrazonoyl chloride (1.50 g), 4-chloro-3-octyloxybenzonitrile (1.30 g), anhydrous iron (III) chloride (0.80 g) and o-dichlorobenzene (5 ml) is stirred at an oil bath temperature of 140° C. for 30 minutes. After cooling, the reaction mixture is dissolved in chloroform (100 ml), washed with dilute hydrochloric acid, dilute aqueous solution of sodium hydroxide and saline in this order, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography using mixed solvent of hexaneethyl acetate as eluent to give 0.80 g of desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05616594 |
|---|
| Source dataset | uspto-grants-1997_04 |
|---|
| ORD ID | ord-48faca2029d943378334cf901ca61c11 |
|---|
| Source note | uspto-grants-1997_04 |
|---|