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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073387Generated: October 31, 2026

Propargyl bromide → 5-Hydroxy-7-propargyloxy-2,2-dimethyl-4-chromanone

https://huagongshe.com/reaction/1073387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
Reactant5,7-Dihydroxy-2,2-dimethylchroman-4-oneHCID 821362—
CatalystPotassium IodideHCID 4875—
SolventMethyl Ethyl KetoneHCID 6569—
Product5-Hydroxy-7-propargyloxy-2,2-dimethyl-4-chromanoneHCID 1459296375%

Reaction Conditions

Temperature0 °C

Reaction Steps

In 60 ml of methyl-ethyl-ketone 4.2 g of 5,7-dihydroxy-2,2-dimethyl-4-chromanone are dissolved, whereupon 3.0 g (22 millimoles) of potassium carbonate, 0.2 g of potassium iodide, and 3.0 g (2.3 ml, 25 millimoles) of propargyl bromide are added and the reaction mixture is reflexed for 4 hours. The inorganic salt is filtered off, the residue is taken up in 100 ml of carbon tetrachloride and extracted twice with 25 ml of a 5% sodium hydroxide solution each. The aqueous-alkaline layer is cooled to 0° C. The aqueous-alkaline layer is cooled to 0° C. The precipitated sodium phenolate salt is filtered off, washed twice with 20 ml of acetone each, and suspended in 25% hydrochloric acid (50 ml). The mixture is stirred at 5° C. for an hour. The precipitated white product is filtered off, washed twice with 20 ml of water each and dried to constant weight. The crude product thus obtained can be directly subjected to further reactions. Thus 3.7 g of the desired compound are obtained, yield 75% Mp.: 122°-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968819
Source datasetuspto-grants-1990_11
ORD IDord-56d9670cf8794dc6a526caf07d1572f8
Source noteuspto-grants-1990_11