Acetic Acid → 2,3,4-Tri-O-acetyl-alpha-D-xylopyranosyl bromide

Acetic acid (6 mL) and a 30% hydrobromic acid-acetic acid solution (25 mL) were put in a 100 mL round bottom flask containing 1,2,3,4-tetra-O-acetyl β-D-xylose (5.0 g, 15.7 mmol) and stirred at room temperature for an hour. Chloroform (100 mL) was poured into the reaction mixture. The resulting mixture was washed with water (100 mL×2) and with a saturated aqueous solution of sodium hydrogen carbonate (100 mL×1), and dried over calcium chloride. The resulting mixture was concentrated to 20 mL. To the resulting mixture, diethyl ether (8 mL) was added, followed by stirring. Petroleum ether (5 mL) was quietly added to the resulting mixture, which was cooled in the freezer for crystallization. The crystals are filtered by suction, washed with cold ether and dried to give the title compound. White acicular crystals. Yield 4.6 g, 87%. The product was unstable at room temperature, and stored in the freezer.

1. washThe resulting mixture was washed with water (100 mL×2) and with a saturated aqueous solution of sodium hydrogen carbonate (100 mL×1)
2. dry with materialdried over calcium chloride
3. concentrationThe resulting mixture was concentrated to 20 mL
4. additionTo the resulting mixture, diethyl ether (8 mL) was added
5. stirringby stirring
6. additionPetroleum ether (5 mL) was quietly added to the resulting mixture, which
7. temperaturewas cooled in the freezer for crystallization
8. filtrationThe crystals are filtered by suction
9. washwashed with cold ether
10. customdried

ORD record

ord-c8d26e96542649a0b3998a8f40d3fb4e

Source dataset

uspto-grants-2007_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07157432B2