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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513112Generated: October 26, 2026

3,5-Dibromophenol → 1,3-Dibromo-5-(cyclopentylmethoxy)benzene

https://huagongshe.com/reaction/1513112

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DibromophenolHCID 12280—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantCyclopentanemethanolHCID 77195—
SolventTetrahydrofuranHCID 8028—
Product1,3-Dibromo-5-(cyclopentylmethoxy)benzeneHCID 67171483—

Reaction Steps

3,5-Dibromophenol (5.0 g; 19.8 mmol), cyclopentane-methanol (2.0 g; 19.9 mmol) and tributylphosphine (8.8 mL; 35.7 mmol) were dissolved in dry THF (250 mL) in a dried reaction flask under an atmosphere of nitrogen. 1,1′-(Azodicarbonyl)dipiperidine (9.01 g; 35.7 mmol) dissolved in dry THF (150 mL) was added to the reaction mixture, which was stirred at room temperature for 16 hours. The reaction mixture was filtered, evaporated to dryness and purified by flash chromatography (heptane→ethyl acetate:heptane 2:3). Yield: 5.68 g; 86%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217086B2
Source datasetuspto-grants-2012_07
ORD IDord-f01b755c80284fc28867413f8208ba48
Source noteuspto-grants-2012_07