HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-(chloromethyl)benzene → 1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4-Methoxyphenylhydrazine hydrochloride | HCID 2723904 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine | HCID 14980564 | 72% |
Reaction Steps
To a suspension under N2 of 4-methoxyphenylhydrazine hydrochloride (41 g, 230 mmol) in methylene chloride (1000 ml) were added diisopropylamine (79.8 g, 612 mmol), 4-chlorobenzyl chloride (40.25 g, 250 mmol) and tetrabutylammonium bromide (22.8 g, 70 mmol), and the resulting mixture was stirred at room temperature for 48 hours. The reaction mixture was then washed with water and brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by chromatography on silica gel (2.5% methanol/methylene chloride), followed by washing of the solid with 10% ethyl ether in hexane and drying in vacuo to provide 43.5 g of 1-(4-chlorobenzyl)-1-(4-methoxyphenyl)hydrazine. mp.55° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399699 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-033cb681b4324a7a82dfee28727d1660 |
| Source note | uspto-grants-1995_03 |