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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388793Generated: October 30, 2026

Aniline → HCID 57640776, compound

https://huagongshe.com/reaction/388793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
ReactantHCID 11582095HCID 11582095—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57640776HCID 57640776—

Reaction Steps

Aryl Bromide (Example 1, 100 mg, 0.25 mmol), aniline (27 uL, 0.30 mmol), Cs2CO3 (163 mg, 0.50 mmol) and Xantphos (43 mg, 0.075 mmol) were diluted with 4 mL of degassed THF. The resulting suspension was degassed for an additional 3 min then Pd2(dba)3 (23 mg, 0.25 mmol) was added giving a dark violet suspension which became dark yellow-orange within a few minutes. The mixture was then refluxed overnight, changing to cloudy orange as the aryl bromide was consumed. The next day the mixture was partitioned with water and ethyl acetate, separated, and the organic layer extracted twice with ethyl acetate. The combined organic layers were dried over MgSO4, filtered, concentrated and purified by preparative HPLC affording the desired product as a white powder. MS found for C21H18ClN3O2S as (M+H)+ 412.0, 414.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377974B2
Source datasetuspto-grants-2013_02
ORD IDord-a3b0ff95d1ca438d96141935bc0ac3ed
Source noteuspto-grants-2013_02