Iodine → 1,6:3,4-Dianhydro-beta-D-talopyranose

HRID 36039

反応式

HRID 36039 の反応式
[C@@H:1]12[O:9][CH2:8][C@@H:6]([O:7]1)[CH:5]=[CH:4][C@@H:2]2[OH:3].II.[OH2:12].N.CO>C(O)(=O)C.C([O-])(=O)C.[Ag+]>[CH2:8]1[O:9][C@@H:1]2[O:7][C@H:6]1[C@@H:5]1[O:12][C@@H:4]1[C@@H:2]2[OH:3]

参加物

7

実験手順

0.13 g (1.00 mmol) of 1,6-anhydro-3,4-dideoxy-β-D-threo-hex-3-enopyranose represented by the above formula [3] was dissolved in 4.6 ml of acetic acid, and further 0.33 g (2.00 mmol) of silver acetate was added thereto. While vigorously stirring the solution at room temperature, 0.27 g (1.05 mmol) of iodine was gradually added to the solution. After the reaction mixture was stirred for 5 hours at room temperature under a nitrogen atmosphere, 40 ml of 25% ammonia water was gradually added to the solution while ice-cooling to convert it to a basic solution. Further 40 ml of methanol was added to the basic solution, which was stirred for overnight at room temperature. Undissolved material was filtered off, and the solvent was removed from the filtrate under reduced pressure. The residue was purified by means of silica gel column chromatography (hexane: ethyl acetate=1: 1), thereby obtaining 1.09 g (yield: 93.8%) of 1,6:3,4-dianhydro-β-D-talopyranose represented by the following formula [4] . This was recrystallized from a hexane-diethyl ether mixed solvent (hexane:diethyl ether=1:4). ##STR13##

後処理

  1. stirringAfter the reaction mixture was stirred for 5 hours at room temperature under a nitrogen atmosphere
  2. temperaturecooling
  3. stirringwas stirred for overnight at room temperature
  4. filtrationwas filtered off
  5. customthe solvent was removed from the filtrate under reduced pressure
  6. customThe residue was purified by means of silica gel column chromatography (hexane: ethyl acetate=1: 1)

出典と根拠

ORDレコード
ord-25c6a4c42cdb4495aec0b0b55501058f
出典データセット
uspto-grants-1995_05
特許番号
US05412111

関連ノート

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