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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180369Generated: November 3, 2026

Diethyl Ether → (5S)-2-(4-bromophenyl)-5-isobutyl-1,3-dioxolan-4-one

https://huagongshe.com/reaction/1180369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantLeucic acid, L-HCID 83697—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventTolueneHCID 1140—
Product(5S)-2-(4-bromophenyl)-5-isobutyl-1,3-dioxolan-4-oneHCID 69473106—

Reaction Steps

(2S)-2-hydroxy-4-methylpentanoic acid (46.4 g, 351 mmol) and 4-bromobenzaldehyde (50 g, 270.2 mmol) were dissolved in 400 ml toluene and pyridinium 4-methylbenzenesulfonate (340 mg, 1.35 mmol) was added. The mixture was refluxed in a Dean-Stark for 24 hours. The mixture was cooled, poured into 500 ml NaHCO3(sat) and 500 ether, the phases were separated and the organic phase washed with 500 ml NaHCO3(sat.) and brine. The organic phase was dried with Na2SO4 and the solvent striped. 400 ml Hexane was added to the resulting solid and the mixture was stirred 1 hour in salt ice bath. The solution was filtered thru Celite, and the solvent removed. (5S)-2-(4-bromophenyl)-5-isobutyl-1,3-dioxolan-4-one (3:2 mixture of cis/trans) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279478B2
Source datasetuspto-grants-2007_10
ORD IDord-1119f1a6e20e41cda8f152f3a4107caa
Source noteuspto-grants-2007_10