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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955352Generated: October 28, 2026

Acetone → HCID 10878747, compound

https://huagongshe.com/reaction/1955352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant(2R)-3-Chloro-1,2-propanediolHCID 148793—
ReactantHCID 178418361HCID 178418361—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 10878747HCID 1087874754%

Reaction Conditions

Temperature60 °C

Reaction Steps

Benzyl alcohol (32.90 g, 0.35 mol) was dropped under ice cooling in a suspension of 60% sodium hydride (5.88 g, 0.155 mol) and DMF (150 ml) After emission of hydrogen gas, therein a DMF solution (15 ml) of (R)-3-chloro-1,2-propanediol (8.535 g, 0.078 mol, optical purity 98.7% e.e.) 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, the insoluble materials were filtered off and the filtrate was condensed in vacuo. Thereto acetone (750 ml) and p-toluenesulfonic acid (0.579 g), were added and the solution was stirred for 5 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 9.267 g of (S)-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-ac3cacdb4c344828883bcd01d3e04b21
Source noteuspto-grants-2000_09