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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955350Generated: November 3, 2026

Acetone → 2,2-Dimethyl-4-((phenylmethoxy)methyl)-1,3-dioxolane

https://huagongshe.com/reaction/1955350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
Reactant3-Chloro-1,2-propanediolHCID 7290—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178418361HCID 178418361—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product2,2-Dimethyl-4-((phenylmethoxy)methyl)-1,3-dioxolaneHCID 8579554%

Reaction Conditions

Temperature60 °C

Reaction Steps

Benzyl alcohol (38.93 g, 0.36 mol) was dropped under ice cooling in a suspension of 60% sodium hydride (7.2 g, 0.103 mol) and DMF (200 ml). After emission of hydrogen gas, therein a DMF solution (15 ml) of 3-chloro-1,2-propanediol (9.95 g, 0.090 mol) was dropped. The reaction temperature was raised to 60° C. and the mixture was stirred under heating for 2 hours. After completion of the reaction the mixture was cooled on ice bath and neutralized with 6% hydrochloric acid. After removal of water and DMF in vacuo, ethyl acetate was added to the residue and the insoluble materials were filtered off and the filtrate was condensed in vacuo. Thereto acetone (1000 ml) and p-toluenesulfonic acid (0.77 g) were added and the solution was stirred for 3 hours at 25° C. After the reaction was over, the mixture was neutralized with triethylamine. After stirring for 5 minutes, acetone was removed in vacuo. The crude product was distilled to give 10.81 g of 4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane (yield 54%, b.p. 110° C. at 0.3 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124479
Source datasetuspto-grants-2000_09
ORD IDord-76a9fa7873234be6aa7aef1178a4f7ac
Source noteuspto-grants-2000_09