HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 1-Thiophenyl-3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranose
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | beta-D-Glucopyranose, 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-, 1,3,4,6-tetraacetate | HCID 2728904 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Thiophenyl-3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranose | HCID 86749129 | — |
Reaction Steps
The product compound [2] (0.31-8.02 g, 0.68-17.7 mmol) is dissolved in 3.2-100 ml of dry dichloromethane, and thiophenol (0.15-3.9 g, 1.36-35.4 mmol) and tin tetrachloride (0.35-9.22 g, 1.36-35.4 mmol) are added and the mixture is stirred until reaction is complete. The reaction mixture is diluted and then washed with saturated sodium bicarbonate solution. Concentration results in the crude product compound [3]. Purification takes place by chromatography on silica gel with an ethyl acetate/isohexane gradient (0.27-71.4 g, 0.54-14.2 mmol, about 80%). FAB-MS: M+H+ =504. NMR data consistent with Nicolaou et al., J. Am. Chem. Soc. 112:3695 (1990) and T. J. Caulfield, Ph.D. Dissertation, the University of Pennsylvania (1991).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05470843 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-71215258f16e4b85b337786d87955c96 |
| Source note | uspto-grants-1995_11 |