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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38384Generated: October 23, 2026

2-Bromopropene → Isoprene 5-isopropenyl-6-methoxy-2,3-dihydro-benzo[1,4]dioxine

https://huagongshe.com/en/reaction/38384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropeneHCID 11202—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acidHCID 22571892—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductIsoprene 5-isopropenyl-6-methoxy-2,3-dihydro-benzo[1,4]dioxineHCID 86600725—

Reaction Steps

To a solution of 2-bromopropene (5.4 ml, 59 mmol) in 200 mL DME was added Pd(Ph3P)4 (3.116, 2.8 mmol). After 30 min 6-methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acid (13.320 g, 58.6 mmol) and K2CO3 (8.099 g, 58.6 mmol) was added. The mixture was warmed to reflux. After 16 hours the mixture was cooled, filtered through a pad of celite and concentrated in vacuo. The residue was dissolved in H2O and extracted with ethyl acetate. The combined organics were washed with saturated NaHCO3, dried over MgSO4, filtered and concentrated in vacuo. Purification via flash chromatography afforded isoprene 5-isopropenyl-6-methoxy-2,3-dihydro-benzo[1,4]dioxine (5.542 g, as an inseparable mixture of product/sm 1:1) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524725B2
Source datasetuspto-grants-2013_09
ORD IDord-4fd92cd7c2664f55914ddd51d2b7f735
Source noteuspto-grants-2013_09