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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584631Generated: November 2, 2026

Hydrogen Bromide → Tri-O-acetyl-D-glucal

https://huagongshe.com/reaction/1584631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantAcetic AnhydrideHCID 7918—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantSodium AcetateHCID 517045—
ReactantAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
CatalystZincHCID 23994—
CatalystCopper SulfateHCID 24462—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductTri-O-acetyl-D-glucalHCID 68830398%

Reaction Steps

Glucose (1.000 g) was suspended in a solution of acetic acid (10 mL) and acetic anhydride (3.606 g, 7.0 equiv) and 1.000 g 31% HBr/acetic acid solution added. The reaction mixture was allowed to stir for 1 h, after which 9.000 g more 31% HBr/acetic acid solution (total of 7.7 equiv HBr) was added and allowed to stir overnight. Sodium acetate was then added (2.700 g) to neutralized the excess HBr, and the reaction mixture was added to a suspension containing pulverized CuSO4 ·5H2O (0.315 g), zinc (12.600 g), water (10 mL), sodium acetate (9.450 g), and acetic acid (5 mL) and the resultant reaction mixture was stirred vigorously for 1.5 h. The solution was then filtered and the solid washed with ethyl acetate (100 mL) and water (100 mL). The organic layer of the filtrate was then washed with NaHCO3 (100 mL) and brine (50 mL), dried (Na2SO4), filtered and the solvent removed under reduced pressure to provide tri-O-acetyl-D-glucal (1.350 g, 98%) as a colorless oil free of impurities as judged by 1H NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932709
Source datasetuspto-grants-1999_08
ORD IDord-126f04cdea02416ba2d0a0c3ce9e82fc
Source noteuspto-grants-1999_08