Benzylamine → 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranose

HRID 2372994

反応式

HRID 2372994 の反応式
C(N)C1C=CC=CC=1.C([O:12][CH:13]1[S:30][CH2:29][C@@H:24]([O:25][C:26](=[O:28])[CH3:27])[C@H:19]([O:20][C:21](=[O:23])[CH3:22])[C@H:14]1[O:15][C:16](=[O:18])[CH3:17])(=O)C>CCOCC>[C:16]([O:15][C@@H:14]1[C@@H:19]([O:20][C:21](=[O:23])[CH3:22])[C@H:24]([O:25][C:26](=[O:28])[CH3:27])[CH2:29][S:30][C@@H:13]1[OH:12])(=[O:18])[CH3:17]

参加物

4

反応物 2

HCID 7504BenzylamineHCID 109912441,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose

生成物 1

HCID 232401882,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranose収率 47.3%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

22 ml (0.2 mol) of benzylamine are added under an inert atmosphere to a solution of 15 g (44.8.10-3 mol) of 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose in 450 ml of ether. After 7 hours at room temperature (15°-25° C.), the reaction mixture is concentrated under reduced pressure and the residue is dissolved in methylene chloride and washed with a 1N solution of hydrochloric acid, a saturated solution of ammonium chloride and then water. The solution obtained is dried over sodium sulfate and the solvent is evaporated off under reduced pressure. 6.2 g (yield: 47%) of the expected product are obtained after purification by chromatography on silica gel using a hexane/ethyl acetate mixture (3/2 v/v) as the eluent, and crystallization from an ethyl acetate/hexane mixture, said product having the following physical characteristics:

後処理

  1. concentrationthe reaction mixture is concentrated under reduced pressure
  2. dissolutionthe residue is dissolved in methylene chloride
  3. washwashed with a 1N solution of hydrochloric acid
  4. customThe solution obtained
  5. dry with materialis dried over sodium sulfate
  6. customthe solvent is evaporated off under reduced pressure

出典と根拠

ORDレコード
ord-bd95c02756634ff68e5e92754f93bce0
出典データセット
uspto-grants-1992_03
特許番号
US05101048

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