Acetic Acid → 1,6-anhydro-3-deoxy-beta-D-threo-hexopyranos-2-ulose

0.47 g (1.50 mmol) of diphenyl diselenide dissolved in 7.5 ml of dry ethanol and 0.11 g (3.00 mmol) of sodium borohydride was gradually added thereto at room temperature. After the reaction mixture was stirred for 5 minutes, 11.6 ml of acetic acid was added to the reaction mixture while ice-cooling. Then, 0.16 g (1.00 mmol of 1,6:3,4-dianhydro-β-D-lyxo-hexopyranos-2-ulose monohydrate represented by the above formula [5'] dissolved in 8 ml of a dry ethanol was added dropwise thereto. After the reaction mixture was stirred for 2 hours while ice-cooling, a temperature thereof was raised to room temperature and diluted by adding 78 ml of ethyl acetate. After a solvent was removed from the reaction solution under reduced pressure, the residue was purified by means of silica gel column chromatography (hexane: ethyl acetate=1:2), thereby obtaining 0.12 g (yield: 80.6%) of 1,6-anhydro-3-deoxy-β-D-threo-hexopyranos-2-ulose represented by the following formula [6]. This was recrystallized from a hexane-diethyl ether mixed solvent. ##STR15##

1. customat room temperature
2. temperaturecooling
3. additionwas added dropwise
4. stirringAfter the reaction mixture was stirred for 2 hours while ice-
5. temperaturecooling
6. additiondiluted
7. customAfter a solvent was removed from the reaction solution under reduced pressure
8. customthe residue was purified by means of silica gel column chromatography (hexane: ethyl acetate=1:2)

ORDレコード

ord-362c638de5734081b3e83f32f07c519e

出典データセット

uspto-grants-1995_05

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05412111