HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993728Generated: October 30, 2026
1,2-Dimethoxyethane → HCID 68897965, compound
https://huagongshe.com/reaction/1993728
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 68899570 | HCID 68899570 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68897965 | HCID 68897965 | 42% |
Reaction Steps
A solution of 0.108 g (1.02 mM) of sodium carbonate in 2 ml of water, 0.055 g (0.0678 mM) of [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) dichloromethane and 0.277 g (1.35 mM) of 4,4,5,5-tetramethyl-2-phenyl-1,2,3-dioxaborolane are added to a solution of 0.31 g (0.678 mM) of 2-chloromethylimidazo[1,2-α]pyridin-8-yl 2,3,4-tri-O-acetyl-5-thio-D-xylopyranoside obtained according to example 31, in 4 ml of DME. The reaction mixture is microwave-heated at 120° C. for 30 minutes. After cooling, water is added and the resulting mixture is extracted with ethyl acetate. The organic phase is dried over sodium sulfate and is concentrated under reduced pressure. The evaporation residue is purified by silica gel chromatography, elution being carried out with a dichloromethane/methanol mixture (97/3; v/v), and then crystallized from ether. The expected product is obtained in the form of a white solid with a yield of 42%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652032B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-f2b8395fbd3d46b0af323c9e2b0a8f1c |
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| Source note | uspto-grants-2010_01 |
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