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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095429Generated: October 30, 2026

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → HCID 59371456, compound

https://huagongshe.com/reaction/2095429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridineHCID 15480236—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 29078034HCID 29078034—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 59371456HCID 5937145657.1%

Reaction Conditions

Temperature99 °C

Reaction Steps

To a solution of 3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridine (118 mg, 0.33 mmol) and 4-[2-(2-phenylethoxy)ethyl]piperidine (77 mg, 0.33 mmol) in anhydrous toluene (2 mL) were added successively sodium tert-butoxide (48 mg, 0.50 mmol, 1.5 equiv.), tris(dibenzylideneacetone)dipalladium(0) (6.1 mg, 6.6 μmol, 0.02 equiv.), and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos; 11.5 mg, 20 μmol, 0.06 equiv.). The mixture was degassed and purged with Ar (3 cycles), then warmed to 98-100° C. for 4 h. After cooling to room temperature, the mixture was diluted with EtOAc, and the solution was washed with brine, dried over Na2SO4, and evaporated. The residue was purified by CC on SiO2 with CH2Cl2/EtOAc 4:1, then 1:1. 3-[[1-(tert-Butoxycarbonyl)-2(S)-pyrrolidinyl]methoxy]-5-[4-[2-(2-phenylethoxy)ethyl]-1-piperidinyl]pyridine (96 mg, 57%) was obtained as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445684B2
Source datasetuspto-grants-2013_05
ORD IDord-de127a7ebd2b4f059eabd571773b12c6
Source noteuspto-grants-2013_05