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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60730Generated: October 28, 2026

Sulfuric Acid → 1-[(2S,4R)-4,5-diacetoxytetrahydrofuran-2-yl]propyl benzoate

https://huagongshe.com/reaction/60730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetic AnhydrideHCID 7918—
Reactant1-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]propyl benzoateHCID 121396390—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
Product1-[(2S,4R)-4,5-diacetoxytetrahydrofuran-2-yl]propyl benzoateHCID 121396291—

Reaction Steps

To a stirred solution of 1-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]propyl benzoate (compound 26a, 6.73 g, 22.0 mmol) and acetic anhydride (11 mL) in acetic acid (44 mL) and chloroform (11 mL) was added concentrated sulfuric acid (200 uL) dropwise. After being stirred at room temperature overnight, the resulted mixture was diluted with EtOAc (100 mL) and washed with a saturated aqueous solution of NaHCO3 (100 mL) three times. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on silica gel (eluting with 1:20 to 1:10 EtOAc in petroleum ether) to afford 5.1 g 1-[(2S,4R)-4,5-diacetoxytetrahydrofuran-2-yl]propyl benzoate (compound 26b) as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09441008B2
Source datasetuspto-grants-2016_09
ORD IDord-cb7352f72ed44d5494c9dc291be2083f
Source noteuspto-grants-2016_09