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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129999Generated: October 27, 2026

Thiophenol → 1-Thiophenyl-3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranose

https://huagongshe.com/reaction/129999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantTin tetrachlorideHCID 24287—
Reactantbeta-D-Glucopyranose, 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-, 1,3,4,6-tetraacetateHCID 2728904—
SolventDichloromethaneHCID 6344—
Product1-Thiophenyl-3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranoseHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05470843
Source datasetuspto-grants-1995_11
ORD IDord-71215258f16e4b85b337786d87955c96
Source noteuspto-grants-1995_11