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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166234Generated: November 3, 2026

HCID 13518532, compound → HCID 13518534, compound

https://huagongshe.com/reaction/2166234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13518532HCID 13518532—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 13518534HCID 1351853455.8%

Reaction Steps

10-(2,3-Dimethoxy-5-methyl-1,4-benzoquinon-6-yl)-decanoyl-D-isoglutamine benzyl ester (3.42 g, 6 mmol) was dissolved in methanol (12 ml) and, the solution was hydrogenated with palladium black at room temperature for 3 hours. After completion of the reaction, the solvent was distilled off and the residue was dissolved in methanol (25 ml). A solution of ferric chloride (2.43 g, 15 mmol) in water (5 ml) was added and the mixture was stirred at room temperature for 10 minutes. The solvent was then distilled off and the residue was dissolved in ethyl acetate (30 ml), washed with water (15 ml×4) and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the residue was chromatographed on a silica gel column. Elution with chloroform-methanol (9:1, v/v), chloroform-acetone-methanol (10:3:2, v/v) and chloroform-methanol-acetic acid (18:2:1, v/v) in that order gave a crude product. The product was recrystallized from ethanol-ethyl ether-petroleum ether to give 10-(2,3-dimethoxy-5-methyl-1,4-benzoquinon-6-yl)-decanoyl-D-isoglutamine (1.61 g), melting at 136°-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943645
Source datasetuspto-grants-1990_07
ORD IDord-1a9d4743ed364f29bcec6c7e6a54907c
Source noteuspto-grants-1990_07