반응 #450535

ord-42ff117433c64abfb9f045636eff755c

반응 방정식

ClCCl
dichloromethane
CC(=O)OC1O[C@H](CCl)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
tetra-O-acetyl-6-chloro-6-deoxy-D-galactopyranose
CC(=O)OC1O[C@H](CCl)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
compound 54
CC(=O)OC1O[C@H](CCl)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
tetra-O-acetyl-6-chloro-6-deoxy-D-galactopyranose
CC(=O)O.NN
hydrazine acetate
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@H](O)O[C@H](CCl)[C@@H]1OC(C)=O
2,3,4-tri-O-acetyl-6-chloro-6-deoxy-α-D-galactopyranose
수율 103.1%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척the resulting solution washed 4 times with water
  2. 2
    건조The organic layer was dried over anhydrous sodium sulfate
  3. 3
    기타evaporated

실험 절차

To a solution of tetra-O-acetyl-6-chloro-6-deoxy-D-galactopyranose (compound 54) (6.36 g, 17.3 mmol) in DMF (60 mL) was added hydrazine acetate (2.4 g, 26.0 mmol). The mixture was stirred for 1 hour at room temperature and then 1 L of dichloromethane was added and the resulting solution washed 4 times with water. The organic layer was dried over anhydrous sodium sulfate and evaporated. Flash column chromatography using hexane-ethyl acetate (1:1) as the eluent gave 2,3,4-tri-O-acetyl-6-chloro-6-deoxy-α-D-galactopyranose (5.79 g). This material was dissolved in 50 mL of dichloromethane and cooled to 0° C. Trichloroacetonitrile (8.93 mL, 89.2 mmol) was added followed by DBU (1.33 mL, 8.9 mmol). This solution was stirred for 1.5 hours and then evaporated. The residue was chromatographed on a silica gel column, eluting with hexane-ethyl acetate (2:1), to provide compound 55 (4.1 g, 51%) as a foam.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05874411uspto-grants-1999_02