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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748701Generated: October 30, 2026

Acetone → HCID 18761932, compound

https://huagongshe.com/reaction/1748701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-DihydroxynaphthaleneHCID 93552—
ProductHCID 18761932HCID 18761932—

Reaction Steps

Into a 1,000 ml two-necked flask equipped with a refluxing condenser, 20.0 g of 2,6-dihydroxynaphthalene (Sigma-Aldrich), 27.0 ml of allyl bromide (Sigma-Aldrich), 103.61 g of K2CO3, and 500 ml of acetone are charged and mixed at room temperature. Then, the temperature was set to 80° C., and the homogeneous mixture thus obtained is refluxed overnight. After finishing the reaction, the reaction mixture is cooled to room temperature and filtered using Celite. Organic solvent is evaporated to obtain a coarse product. A target product is extracted from the coarse product using ethyl acetate, washed three times using water, and dried using MgSO4. MgSO4 is filtered off, and solvents are removed by using an evaporator to obtain an intermediate product (11), 2,6-bis(allyloxy)naphthalene. The reaction scheme of the 1st step is as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150686B2
Source datasetuspto-grants-2015_10
ORD IDord-576b6e9c1c414a318bc41d54e4f34dcf
Source noteuspto-grants-2015_10