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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493071Generated: October 30, 2026

Pyridine → HCID 10850422, compound

https://huagongshe.com/reaction/1493071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAnilineHCID 6115—
ReactantSodium DithioniteHCID 24489—
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—
SolventWaterHCID 962—
ProductHCID 10850422HCID 1085042242.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

Titanium tetrachloride (2.58 ml, 23.4 mmol) was added dropwise to a solution of pyridine (7.60 ml, 93.6 mmol) in 1,2-dichloroethane (40 ml) and, after completion of the addition, the reaction mixture was heated under reflux for 30 minutes in an argon atmosphere. After cooling of the reaction mixture, a solution of 3,5,6-trimethyl-2-(2-methyl-2-propenyl)-1,4-benzoquinone (2.40 g, 11.7 mmol) and aniline (3.35 mi, 35.1 mmol) in 1,2-dichloroethane (5 ml) was added thereto and the mixture was stirred at 90° C. for 2 hours in an argon atmosphere. The reaction mixture was cooled and filtered through Cerite and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate, 98:2. The resulting compound was dissolved in tetrahydrofuran (10 ml) and to the solution was added a solution of sodium hydrosulfite (12 g, 69 mmol) in water (30 ml). The mixture was stirred at room temperature for 30 minutes. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The extract was combined with the organic phase and the mixture was washed with water and dried and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (hexane-ethyl acetate, 95:5) to obtain the desired compound as oil (1.41 g, yield: 42.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05376681
Source datasetuspto-grants-1994_12
ORD IDord-0e50fa342cd742b6a1d6840de7792216
Source noteuspto-grants-1994_12