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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387590Generated: November 1, 2026

Allyl bromide → HCID 67151185, compound

https://huagongshe.com/reaction/2387590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant2-Propen-1-ol, 2-methyl-3-(4-methylphenyl)-, (2E)-HCID 15683411—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67151185HCID 6715118595%

Reaction Conditions

Temperature5 °C

Reaction Steps

Solid potassium tert-butylate (47 g, 0.411 mol) was added portion-wise to a solution of E-3-(4-methylphenyl)-2-methyl-2-propen-1-ol (68.05 g, 0.420 mol) in dry THF (800 ml) at room temperature under nitrogen (exothermic to 30° C.). After 1 more hour at room temperature, the reaction was cooled to 5° C. and tetra butyl ammonium iodide (7.9 g, 0.021 mol) was added followed by allyl bromide (102.65 g, 0.840 mol) drop-wise. The reaction was warmed up to room temperature overnight and poured onto water (800 ml). The reaction was extracted twice with ethyl acetate. Each organic phase was washed with water and brine. Combined extracts were dried over solid anhydrous sodium sulfate. The solid was filtered off, rinsed with diethyl ether and the solvents were removed under vacuum. The product was purified by distillation under vacuum through a 20-cm Widmer column. 79 g of the desired product were obtained (yield=93%). B.P.=82° C./0.001 mbar

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268895B2
Source datasetuspto-grants-2012_09
ORD IDord-b11cc0977e914d3d80169bad418f489d
Source noteuspto-grants-2012_09