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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095454Generated: November 2, 2026

3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridine → HCID 59371470, compound

https://huagongshe.com/reaction/2095454

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridineHCID 15480236—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 56829989HCID 56829989—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 59371470HCID 5937147064%

Reaction Conditions

Temperature99 °C

Reaction Steps

To a solution of 3-bromo-5-[[1-(tert-butoxycarbonyl)-2(R)-pyrrolidinyl]methoxy]pyridine (254 mg, 0.71 mmol) and 4-[2-(4-methylbenzyloxy)ethyl]piperidine (182 mg, 0.78 mmol, 1.1 equiv.) in anhydrous toluene (2 mL) were added successively sodium tert-butoxide (102 mg, 1.07 mmol), tris(dibenzylideneacetone)dipalladium(0) (13.0 mg, 14 μmol, 0.02 equiv.), and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos; 24.7 mg, 43 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. The product (231 mg, 64%) was obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445684B2
Source datasetuspto-grants-2013_05
ORD IDord-89d9d99b171b42bb886955a3a0a617b0
Source noteuspto-grants-2013_05