Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451589Generated: October 26, 2026

Dimethylformamide → 15-Methoxymethoxy-13-pentadecyne

https://huagongshe.com/reaction/1451589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPropargyl alcoholHCID 7859—
Reactant1-BromododecaneHCID 8919—
ReactantSodium hydrideHCID 24758—
ReactantHypochlorous acid, ethyl esterHCID 136439—
Product15-Methoxymethoxy-13-pentadecyneHCID 21849230—

Reaction Steps

Propargyl alcohol (3.00 g) was portionwise added to a mixed solution of 2.256 g of sodium hydride and 30 ml of dry dimethylformamide under ice-cooling under a nitrogen atmosphere. The mixture was stirred at room temperature for 30 minutes. The mixture was ice-cooled again and 5.175 g of chloro methyl methyl ether was portionwise added thereto. The mixture was stirred at room temperature overnight. Then, 4.284 g of sodium hydride was added thereto under ice-cooling and the mixture was heated to room temperature, followed by stirring for 30 minutes. The reaction mixture was ice-cooled again and a solution of 26.68 g of lauryl bromide in 20 ml of dry dimethylformamide was portionwise added thereto. The mixture was stirred at room temperature overnight. The reaction mixture was poured into ice water and extracted three times with ethyl acetate. The ethyl acetate layer was washed with saturated brine and dried over magnesium sulfate anhydride. The solvent was distilled away under reduced pressure and the residue was purified by silica gel column chromatography to give 12.374 g of 15-methoxymethoxy-13-pentadecyne.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604229
Source datasetuspto-grants-1997_02
ORD IDord-eed07bebe70942598ad989799d895322
Source noteuspto-grants-1997_02