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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373147Generated: October 30, 2026

Water → HCID 68617428, compound

https://huagongshe.com/reaction/2373147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenothiazineHCID 7108—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 86600087HCID 86600087—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventTolueneHCID 1140—
ProductHCID 68617428HCID 68617428—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of tris(dibenzylideneacetone) dipalladium (Pd2(dba)3) (0.13 g, 0.14 mmol) and bis(diphenylphosphino)ferrocene (DPPF) (0.10 g, 0.17 mmol) in dry toluene (20 ml) under nitrogen atmosphere was added 4-[2-(4-bromophenyl)vinyl]-N, N-bis(4-butylphenyl)aniline (2.60 g, 4.83 mmol) at room temperature, and the resultant mixture was stirred for 10 min. Sodium tert-butoxide (1.3 g) and phenothiazine (0.96 g, 4.83 mmol) were then added to this solution, which was then stirred at 90° C. overnight under nitrogen. The reaction mixture was poured into water (60 ml), extracted three times with ether (100 ml×3) and dried over anhydrous magnesium sulfate. The product was purified by flash column chromatography using 2% ethyl acetate in hexane as eluant and was isolated in 60% (1.91 g) yield as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459106B2
Source datasetuspto-grants-2008_12
ORD IDord-9b629f2a3fed4e4a9ee786558ad440a3
Source noteuspto-grants-2008_12