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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334552Generated: October 29, 2026

Carbon tetrabromide → 1-(3-Bromoprop-1-yn-1-yl)-4-fluorobenzene

https://huagongshe.com/reaction/334552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant3-(4-Fluorophenyl)prop-2-yn-1-olHCID 2782698—
SolventDichloromethaneHCID 6344—
Product1-(3-Bromoprop-1-yn-1-yl)-4-fluorobenzeneHCID 1056052499.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-(4-fluorophenyl)prop-2-yn-1-ol (1 g, 6.80 mmol) in DCM (13.6 mL) under N2 was cooled in a ice bath at 0° C. 2.70 g (8.2 mmol, loading 3 mmol/g) of triphenylphosphine polymer supported was then added followed by 2.70 g (8.2 mmol) of carbon tetrabromide. The reaction mixture was stirred 15 min at 0° C. and warmed to room temperature for 90 min. After filtration through celite, the solvent was evaporated under reduce pressure. The crude product was purified by flash chromatography (prepacked 25 g silicagel column, DCM 100% as eluent) to afford 1.44 g of 1-(3-bromoprop-1-ynyl)-4-fluorobenzene as a yellow oil (Yield: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-be071408f1204465bad74f652f817451
Source noteuspto-grants-2014_11