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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561841Generated: October 26, 2026

Tributylphosphine → 2-(3-(4-Bromophenyl)propoxy)-3-chloro-1,4-difluorobenzene

https://huagongshe.com/reaction/561841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant2-Chloro-3,6-difluorophenolHCID 2773561—
Reactant3-(4-Bromophenyl)propan-1-olHCID 10560614—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product2-(3-(4-Bromophenyl)propoxy)-3-chloro-1,4-difluorobenzeneHCID 66760972—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-(4-Bromophenyl)propan-1-ol from the previous step (1 eq.) and 2-chloro-3,6-difluorophenol (1 eq.) were taken up in freshly deoxygenated toluene (0.3 M). To this solution was then added 1,1′-(azodicarbonyl)-dipiperidine (1.2 eq.) and finally tributylphosphine (1.2 eq.). The resulting yellow solution was heated at 80° C. for 2 h. The reaction mixture was cooled to RT, diluted with ether, and washed with 1 N aq. NaOH. The aqueous wash was back extracted with ether and the combined organic extracts were dried over MgSO4. Filtration and concentration of the filtrate in vacuo afforded a yellow semi-solid. Purification of the crude product thus obtained by way of flash chromatography (SiO2, Hex→15:1 (v/v) Hex:EtOAc) afforded the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063105B2
Source datasetuspto-grants-2011_11
ORD IDord-3113e977140649649adde3ee3d4a5b46
Source noteuspto-grants-2011_11