p-Toluenesulfonic acid → 2-[(4S)-2,2-diethyl-1,3-dioxolan-4-yl]ethanol

In 150 ml of 3,3-dimethoxypentane was dissolved 25 g of (S)(-)-butanetriol, and 0.1 g of p-toluenesulfonic acid was added to the solution. The solution was stirred for 16 hr to conduct a reaction. The resultant reaction mixture was poured into a saturated aqueous solution of sodium hydrogencarbonate, the reaction product was extracted with an ether, and the extract was washed with a saturated saline solution. The solvent was distilled off from the extract as washed, and the resultant residue was purified by a silica gel column chromatography through the use of hexane-ethyl acetate as a developing solvent to obtain 26.5 g of (S)-2,2-diethyl-4-(2-hydroxyethyl)-1,3-dioxolane. The whole quantity of the product was dissolved in 500 ml of benzene, and 24 g of imidazole, 100 g of triphenylphosphine and 40 g of iodine were added to the solution. The mixture was stirred for 2 hr and then poured into ice water. The reaction product was extracted with an ether, and the extract was well washed with a 10% aqueous solution of sodium thiosulfate and dried over magnesium sulfate. The solvent was removed from the dried reaction product by distillation, and the resultant residue was purified by a silica gel column chromatography through the use of hexane-ethyl acetate as a developing solvent to obtain 31 g of (S)-2,2-diethyl-4-(2-iodoethyl)-1,3-dioxolane.

1. additionwas added to the solution
2. customa reaction
3. customThe resultant reaction mixture
4. extractionthe reaction product was extracted with an ether
5. washthe extract was washed with a saturated saline solution
6. distillationThe solvent was distilled off from the
7. extractionextract
8. washas washed
9. customthe resultant residue was purified by a silica gel column chromatography through the use of hexane-ethyl acetate as a developing solvent

ORD record

ord-b9d8d477b9d34de1b83f98731d168a38

Source dataset

uspto-grants-1996_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05480580