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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450930Generated: October 29, 2026

Carbon tetrabromide → HCID 20482698, compound

https://huagongshe.com/reaction/450930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant{3-[(Prop-2-en-1-yl)oxy]phenyl}methanolHCID 28065595—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20482698HCID 2048269824%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of (3-allyloxy-phenyl)-methanol (Tetrahedron (2000), 56(13), 1873-1882) (1.07 g, 6.49 mmol) in THF (7 mls) at 3° C. was added carbon tetrabromide (2.69 g, 8.11 mmol) then triphenylphosphine (2.13 g, 8.11 mmol) in THF (2 mls). The reaction mixture was stirred at 5° C. for 1 hour. The reaction mixture was filtered and concentrated in vacuo. The residue was washed with pentane to give a yellow solid which was purified by column chromatography on silica gel, eluting with pentane:ethyl acetate, 100:0, to 95:5 to afford the title compound as a pale yellow oil in 24% yield, 350 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486992B2
Source datasetuspto-grants-2013_07
ORD IDord-bee3443ecee146f3b0f8278866d8a4f6
Source noteuspto-grants-2013_07