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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354293Generated: October 30, 2026

Hydrochloric Acid → HCID 68745664, compound

https://huagongshe.com/reaction/2354293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-4-ethylbenzeneHCID 12231560—
ReactantHCID 57616156HCID 57616156—
SolventDimethylformamideHCID 6228—
ProductHCID 68745664HCID 6874566478.5%

Reaction Steps

To a solution of 3-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-4-methyl-1H-indole (150 mg) in N,N-dimethylformamide (2 mL) was added 55% sodium hydride (12 mg) under ice-cooling, and the mixture was stirred at the same temperature for 15 minutes. To this mixture was added 4-ethylbenzyl bromide (55 mg) at the same temperature, and the mixture was stirred at the same temperature for 15 minutes, and stirred at room temperature for 1 hour. The reaction mixture was poured into 0.5 mol/L hydrochloric acid, and the resulting mixture was extracted with diethylether. The extract was washed with water and brine successively, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. The residue was washed with a mixed solvent of n-hexane and diethyl ether (10/1), and dried under reduced pressure to give 3-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-1-(4-ethyl-benzyl)-4-methyl-1H-indole (139 mg). This material (125 mg) was dissolved in a mixed solvent of methanol (2 mL) and tetra hydrofuran (2 mL). To the solution was added 10% palladium-carbon powder (50 mg), and the mixture was stirred at room temperature under a hydrogen atmosphere for 4 hours. The insoluble material was removed by filtration, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=8/1) to give the title compound (58 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750145B2
Source datasetuspto-grants-2010_07
ORD IDord-e213a3a512994468818a56b538b038bf
Source noteuspto-grants-2010_07