Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660679Generated: October 31, 2026

10-Methyl-10H-phenothiazine-3-carbaldehyde → HCID 67431933, compound

https://huagongshe.com/reaction/1660679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant10-Methyl-10H-phenothiazine-3-carbaldehydeHCID 617826—
ReactantTetraethyl [[1,1'-biphenyl]-4,4'-diylbis(methylene)]bis(phosphonate)HCID 635132—
ReactantPotassium tert-butoxideHCID 23665647—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67431933HCID 67431933—

Reaction Steps

0.80 g (7.1 mmol) of potassium tert-butoxide and then 1.82 g (3.3 mmol) of 10-methylphenothiazine-3-carbaldehyde were added under nitrogen at room temperature with stirring to a solution of 1.42 g (3.14 mmol) of diethyl[4′-(diethoxyphosphoryl-methyl)biphenyl-4-ylmethyl]phosphonate (U.S. Pat. No. 3,984,399, Example 2, column 29, line 58-66) in 32 ml of dimethyl sulfoxide dried over molecular sieve. After stirring at room temperature for four hours, the reaction solution was diluted with 70 ml of methanol and stirred for a further 15 min. The precipitate was filtered off, washed with 172 ml of methanol and dried at 35° C. under reduced pressure. The crude product (1.70 g) was recrystallized in 255 ml of N-methylpyrrolidone. After the solvent residues had been removed at 225° C. under high vacuum, 0.98 g (50% of theory) of analytically pure yellow solid having a melting point of 380° C. was obtained, whose solution in N-methylpyrrolidone fluoresced at λ=576 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08029919B2
Source datasetuspto-grants-2011_10
ORD IDord-a646f96522d044abbcfc5ecba75467c6
Source noteuspto-grants-2011_10