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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720318Generated: November 2, 2026

Chlorobenzene → HCID 22417752, compound

https://huagongshe.com/reaction/1720318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantTin tetrachlorideHCID 24287—
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Methyl-3-nitrobenzyl alcoholHCID 90289—
ProductHCID 22417698HCID 2241769824%
ProductHCID 22417752HCID 2241775241%

Reaction Steps

A mixture of 25 g (0.15 mol) of 2-methyl-3-nitrobenzyl alcohol and 25 ml (0.22 mol) of tintetrachloride in 250 ml of chlorobenzene is refluxed for 3 hours with stirring. After cooling 50 ml of N-methylpiperazine is slowly instilled. The precipitate is suctioned off and washed several times with ethyl acetate. The combined filtrates are dried on sodium sulfate and concentrated by evaporation and the temperature must not rise above 160° C. The residue (39 g) with a mixture of 33 parts of cyclohexane and 1 part of ethyl acetate is subjected twice to a pressure column chromatography. Thus 9.3 g (24%) of 2-(2-chlorobenzyl)-6-nitrotoluene, melting point 54°-56° C., and 16 g (41%) of 2-(4-chlorobenzyl)-6-nitrotoluene, melting point 62°-63° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506234
Source datasetuspto-grants-1996_04
ORD IDord-feb2159c07544fabb4d01d70f87501b9
Source noteuspto-grants-1996_04