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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466342Generated: October 26, 2026

Hydrochloric Acid → 1,3-Bis(2,2-dimethyl-4-pentenoyloxy)-propane

https://huagongshe.com/reaction/466342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,3-DibromopropaneHCID 8001—
ReactantSodium HydroxideHCID 14798—
Reactant2,2-Dimethyl-4-pentenoic acidHCID 140065—
SolventWaterHCID 962—
Product1,3-Bis(2,2-dimethyl-4-pentenoyloxy)-propaneHCID 1974552668.5%

Reaction Steps

To a mixture of 2.6 g (0.02 mole) of 2,2-dimethyl-4-pentenoic acid (XII) and 50 ml of hexamethylphosporic triamide a solution of 1.2 g (0.03 mole) of sodium hydroxide in 3.6 ml of water is added. The reaction mixture is stirred at room temperature for 1 hour and then 1.2 ml (2.4 g, 0.012 mole) of 1,3-dibromopropane are added. The mixture is stirred at room temperature for 4 hours, then poured onto 100 ml of 5% aqueous hydrochloric acid and extracted twice with 50 ml of diethyl ether each. The organic phase is washed twice with 25 ml of water each, dried over sodium sulfate and the solvent is distilled off under reduced pressure. The crude product thus obtained is purified by chromatography on a silica gel column eluted with a 7:3 mixture of hexane and diethyl ether. Thus 2.03 g of the desired compound are obtained in the form of a colourless oil. Yield: 68.5%. According to TLC chromatography using the above-specified eluent Rf =0.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155260
Source datasetuspto-grants-1992_10
ORD IDord-d0e06574e7ca4cc7951fc21f74d5cc03
Source noteuspto-grants-1992_10