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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266721Generated: October 28, 2026

Thionyl Chloride → HCID 15813206, compound

https://huagongshe.com/reaction/266721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 15813205HCID 15813205—
SolventPyridineHCID 1049—
ProductHCID 15813206HCID 15813206—

Reaction Conditions

Temperature60 °C

Reaction Steps

Dimethyl 6-methyl-4-methylamino-2-(4-trifluommethyl-phenyl)cyclohexa-3,5-diene-1,3-dicarboxylate (3) ##STR8## 10.0 g (25 mmol) of dimethyl 6-hydroxy-6-methyl-4-methylamino-2-(4-trifluoromethylphenyl)-cyclohex-3-ene-1,3-dicarboxylate (preparation analogous to Example II) are heated to 60° C. in 100 ml of pyridine and treated with 2.5 ml of thionyl chloride. The mixture is stirred at 60° C. for 10 minutes and concentrated, and the residue is taken up in methylene chloride, washed three times with water, dried and concentrated. The residue is grossly purified on 200 g of silica gel (petroleum ether/AcOEt=3:1) and then separated by MPLC (methylene chloride/AcOEt=30:1). Two fractions are obtained. 224 mg (2.3%) of dimethyl 4-methyl-6-methylamino-2-(4-trifluoromethylphenyl)-cyclohexa-3,6-diene-1,3-dicarboxylate (non-polar isomer (2)) crystallize from ether/petroleum ether. From the 2nd fraction, 2.29 g (22%) of the polar isomer, dimethyl 6-methyl-4-methylamino-2-(4-trifluoromethylphenyl)-cyclohexa-3,5-diene-1,3-dicarboxylate (3) are precipitated from AcOEt as the hydrochloride (Rf =0.47 (c)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652264
Source datasetuspto-grants-1997_07
ORD IDord-08fc2c1891bd45acb05ea19dafbad52f
Source noteuspto-grants-1997_07