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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307748Generated: November 1, 2026

Toluene → HCID 10188276, compound

https://huagongshe.com/reaction/2307748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantBenzyl bromoacetateHCID 62576—
ReactantHCID 11114005HCID 11114005—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventDimethylacetamideHCID 31374—
ProductHCID 10188276HCID 10188276—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture that consists of 54.1 g (100 mmol) of 2,3,4,6-tetra-O-pivaloyl-glucopyranose, 1.39 g (5 mmol) of tetrabutylammonium chloride and 11.22 g of potassium-t-butoxide (100 mmol) in 500 ml of dimethylacetamide is cooled to 0° C. At 0° C., 34.36 g (150 mmol) of 2-bromoacetic acid benzyl ester is added in drops over 20 minutes while being stirred vigorously. It is stirred for one hour at 0° C. Then, 250 ml of toluene is added thereto, solid is filtered out, it is evaporated to the dry state in a vacuum, the residue is taken up in 500 ml of ethanol, mixed with 5 g of palladium (10%) on activated carbon and hydrogenated until the hydrogen absorption is completed. Catalyst is filtered out, it is rewashed with a little ethanol and the combined organic solutions are evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: dichloromethane/n-hexane/ethanol/acetic acid=20:5:3:0.5). The product-containing fractions are concentrated by evaporation, dissolved in 400 ml of ethyl acetate and shaken out three times with 200 ml of water. Then, the organic phase is separated and evaporated to the dry state in a vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831164B2
Source datasetuspto-grants-2004_12
ORD IDord-434855ccbdb84ebcacc1513550ed5d18
Source noteuspto-grants-2004_12