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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969196Generated: October 27, 2026

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

https://huagongshe.com/reaction/1969196

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 numberUS08426473B2
Source datasetuspto-grants-2013_04
ORD IDord-37160d9c81c2468d92ca4e823608e2bd
Source noteuspto-grants-2013_04