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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307745Generated: October 31, 2026

Potassium Carbonate → HCID 10231749, compound

https://huagongshe.com/reaction/2307745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantBenzyl bromoacetateHCID 62576—
ReactantHCID 12997455HCID 12997455—
CatalystTetramethylammonium chlorideHCID 6379—
SolventDiglymeHCID 8150—
ProductHCID 10231749HCID 10231749—

Reaction Conditions

Temperature10 °C

Reaction Steps

A mixture that consists of 51.66 g (100 mmol) of 2,3,4,6-tetra-O-pivaloyl-mannopyranose, 0.55 g (5 mmol) of tetramethylammonium chloride and 82.93 g (600 mmol) of fine-powder potassium carbonate in 350 ml of diethylene glycol dimethyl ether is cooled to 10° C. At 10° C., 36.65 g (160 mmol) of 2-bromoacetic acid benzyl ester is added in drops within 10 minutes while being stirred vigorously. It is stirred for two hours at 10° C. 250 ml of MTB (methyl-tert-butyl ether) is added, solid is filtered out, and the filtrate 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 hydrogen absorption is completed. Catalyst is filtered out, it is rewashed with ethanol, and the combined 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-b4af431218f94c33ab3f36dbd8e75b49
Source noteuspto-grants-2004_12