beta-D-Glucose pentaacetate → HCID 12085619, compound

HRID 1982829Notes

Reaction equation

HRID 1982829 reaction equation
[OH:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[CH2:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([NH2:11])=[O:10])=[CH:7][CH:6]=1.C(O[C@@H:22]1[O:39][C@H:38]([CH2:40][O:41][C:42](=[O:44])[CH3:43])[C@@H:33]([O:34][C:35](=[O:37])[CH3:36])[C@H:28]([O:29][C:30](=[O:32])[CH3:31])[C@H:23]1[O:24][C:25](=[O:27])[CH3:26])(=O)C>C1(C)C=CC=CC=1>[C:25]([O:24][C@@H:23]1[C@@H:28]([O:29][C:30](=[O:32])[CH3:31])[C@H:33]([O:34][C:35](=[O:37])[CH3:36])[C@@H:38]([CH2:40][O:41][C:42](=[O:44])[CH3:43])[O:39][C@H:22]1[O:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[CH2:4][C:5]1[CH:13]=[CH:12][C:8]([C:9](=[O:10])[NH2:11])=[CH:7][CH:6]=1)(=[O:27])[CH3:26]

Participants

4

Procedure

To a suspension of 4-(2-hydroxybenzyl)benzamide (0.063 g) and 1,2,3,4,6-penta-O-acetyl-β-D-glucopyranose (0.33 g) in toluene (3 mL) was added boron trifluoride diethyl ether complex (0.11 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=4/1) to give 2-(4-carbamoylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside. To a solution of the obtained 2-(4-carbamoylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside in methanol (5 mL) was added sodium methoxide (0.005 g), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: ethyl acetate/ethanol=5/1) to give 2-(4-carbamoylbenzyl)phenyl β-D-glucopyranoside (0.068 g).

Workup

  1. additionwas added boron trifluoride diethyl ether complex (0.11 mL)
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customthe residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=4/1)

Sources & evidence

ORD record
ord-93557f1a7ad84819be3c195b522ea7df
Source dataset
uspto-grants-2009_06
Patent number
US07541341B2

Reaction notes

Loading…