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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660690Generated: October 31, 2026

Tetraethyl [[1,1'-biphenyl]-4,4'-diylbis(methylene)]bis(phosphonate) → HCID 72337841, compound

https://huagongshe.com/reaction/1660690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethyl [[1,1'-biphenyl]-4,4'-diylbis(methylene)]bis(phosphonate)HCID 635132—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86648279HCID 86648279—
SolventChloroformHCID 6212—
ProductHCID 72337841HCID 72337841—

Reaction Steps

0.93 g (8.1 mmol) of potassium tert-butoxide and then 2.70 g (7.16 mmol) of 10-mesityl-5,5-dioxophenothiazine-3-carbaldehyde (example 35b) were added at room temperature with stirring under nitrogen to a solution of 1.63 g (3.58 mmol) of diethyl[4′-(diethoxyphosphorylmethyl)biphenyl-4-ylmethyl]phosphonate (U.S. Pat. No. 3,984,399, example 2, column 29, lines 58-66) in 40 ml of dimethyl sulfoxide which has been dried over a molecular sieve. After stirring at room temperature for 4 h, the reaction solution was diluted with 200 ml of methanol and stirred for a further 1 h. The precipitate was filtered off, washed with 100 ml of methanol, stirred up again in 300 ml of methanol, filtered again and dried at 35° C. under reduced pressure. The crude product (2.90 g) was recrystallized twice from dimethylformamide and once from chlorobenzene. The crystals were filtered off with suction, washed successively with chlorobenzene and ethanol, filtered off with suction and dried at 80° C. under reduced pressure. After the removal of solvent residues under high vacuum (2×10−5 mbar) at 250° C., 0.98 g (30% of theory) of analytically pure luminous yellow microcrystals having an m.p. of >350° C. were obtained, whose solution in chloroform fluoresced at λ=456, 485 (S), 522 (S) nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08029919B2
Source datasetuspto-grants-2011_10
ORD IDord-37baab55a49a4176b9597daed0f71b67
Source noteuspto-grants-2011_10