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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234280Generated: October 31, 2026

Pyridine → HCID 10829037, compound

https://huagongshe.com/reaction/234280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-ChloroanilineHCID 7812—
Reactant2,3,5-Trimethyl-6-(2-methylprop-2-en-1-yl)cyclohexa-2,5-diene-1,4-dioneHCID 318840—
CatalystTitanium TetrachlorideHCID 24193—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 10829037HCID 1082903796%

Reaction Conditions

Temperature90 °C

Reaction Steps

Titanium tetrachloride (2.42 ml, 22.1 mmol) was added dropwise to a solution of pyridine (7.13 ml, 88.2 mmol) in 1,2-dichloroethane (40 ml) and, after completion of addition, the reaction mixture was heated under reflux minutes in an argon atmosphere. After cooling of the reaction mixture, to the mixture was added a solution of 3,5,6-trimethyl-2-(2-methyl-2-propenyl)-1,4-benzoquinone (3.00 g, 14.7 mmol) and p-chloroaniline (5.62 g, 44.1 mmol) in 1,2-dichloroenhane (20 ml) and the mixture was stirred 90° C. for 45 minutes in an argon atmosphere. The reaction mixture was cooled and filtered through Cerite and the filtrate was washed with a saturated saline solution, dried and concentrated. The residue was purified by silica gel column chromatography (hexane-ethyl acetate, 93:7) to obtain the desired compound as oil (4.43 g, yield: 96.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594154
Source datasetuspto-grants-1997_01
ORD IDord-a08b7c6307b54c0da120ce99876fcd06
Source noteuspto-grants-1997_01