تفاعل #58014

ord-eb77f61792b84d4e85c3a0623c96c0f5

معادلة التفاعل

C[C@@H]1OC(O)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1
2,3,4-tri-O-benzyl-L-fucopyranose
C[C@@H]1OC(O)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1
2.3.4-Tri-O-benzyl-L-fucopyranose
C[C@@H]1OC(O)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1
compound 6
C[C@@H]1OC(O)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1
2.3.4-Tri-O-benzyl-L-fucopyranose
O=C(Cl)c1ccc([N+](=O)[O-])cc1
p-nitrobenzoyl chloride
O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoyl chloride
O=C(Cl)c1ccc([N+](=O)[O-])cc1
compound 7
O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoyl chloride
C[C@@H]1O[C@@H](OC(=O)c2ccc([N+](=O)[O-])cc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1
material
المردود 80.0%
C[C@@H]1O[C@@H](OC(=O)c2ccc([N+](=O)[O-])cc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1
2,3,4-Tri-O-benzyl-1-O-p-nitrobenzoyl-α-L-fucopyranose
المردود 80.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe column purification
  2. 2
    ترشيحsimply filtered through a short column of silica gel
  3. 3
    أخرىThis removed the color and other polar material
  4. 4
    أخرىThis procedure furnished

الإجراء التجريبي

Since both the α and β isomers yielded the same β-bromide (compound 9), it was decided to skip the column purification and instead use the mixture as such. In this case, 2,3,4-tri-O-benzyl-L-fucopyranose (compound 6) (25 g, 55 mmol) was treated with p-nitrobenzoyl chloride (compound 7) as described above and the crude material (33.0 g) was dissolved in CH2Cl2 (100 mL) and simply filtered through a short column of silica gel. This removed the color and other polar material. This procedure furnished the anomeric mixture of esters (compound 8) as a gummy material (25.7 g, yield 80%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07422733B2uspto-grants-2008_09