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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660672Generated: October 31, 2026

Potassium Carbonate → HCID 20781554, compound

https://huagongshe.com/reaction/1660672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant3,7-dibromo-10-methylphenothiazineHCID 10915650—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 20781554HCID 20781554—

Reaction Steps

2.50 g (6.7 mmol) of 3,7-dibromo-10-methylphenothiazine (C. Bodea and M. Terdic, Acad. Rep. Rom. 1962, 13, 81-87), 1.85 g (14.9 mmol) of 98% phenylboronic acid, 0.11 g (0.14 mmol) of bis(triphenylphosphine)palladium dichloride and 1.03 g (7.4 mmol) of potassium carbonate were heated to boiling (75° C.) under reflux under nitrogen for 5 hours in 55 ml of dimethoxyethane and 28 ml of water. The reaction mixture was cooled to room temperature and stirred further overnight. The precipitate was filtered off with suction, washed successively with 125 ml of ethanol and hot water and dried at 70° C. under reduced pressure. The crude product (2.30 g) was heated to boiling under reflux in cyclohexane for two hours. After the hot suspension had been filtered, the residue was dried, dissolved in 40 ml of methylene chloride and filtered through a silica-gel-filled glass fit. After the solvent had been removed, 1.05 g (43% of theory) of light yellow, analytically pure solid having a melting point of 239-241° C. were obtained, whose solution in chloroform fluoresced at λ=464 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08029919B2
Source datasetuspto-grants-2011_10
ORD IDord-feac67004ef7494a8768dbddaa96766a
Source noteuspto-grants-2011_10