Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162018Generated: October 28, 2026

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → 1-(5-Nitro-1-benzofuran-7-yl)-3-(trifluoromethyl)piperazine

https://huagongshe.com/reaction/1162018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant2-(Trifluoromethyl)piperazineHCID 18519725—
ReactantHCID 21864764HCID 21864764—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventO-XyleneHCID 7237—
Product1-(5-Nitro-1-benzofuran-7-yl)-3-(trifluoromethyl)piperazineHCID 66892016444.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 7-iodo-5-nitro-1-benzofuran (231.4 mg, 0.08 mmol) the following was added: Xantphos (92.6 mg, 0.16 mmol), Pd2 dba3 (36.6 mg, 0.04 mmol), sodium tert-butoxide (215.4 mg, 2.24 mmol), 2-(trifluoromethyl)piperazine (148.1 mg, 0.96 mmol; Intermediate 45) and xylene (23 mL). The resulting mixture was stirred at 100° C. for 3 days. Filtration through Celite and purification by flash chromatography, using EtOAc:heptane (1:1) as eluent, furnished 1-(5-nitro-1-benzofuran-7-yl)-3-(trifluoromethyl)piperazine (112 mg, 44% yield). HPLC 90%, RT=1.648 min (System A; 10-97% MeCN over 3 min), MS (ESI+) m/z 316 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820675B2
Source datasetuspto-grants-2010_10
ORD IDord-5c9f574fd9e94c288783540fd302b1d1
Source noteuspto-grants-2010_10