HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544887Generated: October 26, 2026
1,2-Dimethoxyethane → HCID 67196905, compound
https://huagongshe.com/reaction/544887
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | 4-(Difluoromethoxy)benzeneboronic acid | HCID 23082146 | — |
| Reactant | 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)indole-3-carboxaldehyde | HCID 71500259 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Catalyst | Rhodium, dicarbonyl(2,4-pentanedionato)- | HCID 5377512 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67196905 | HCID 67196905 | — |
Reaction Steps
A mixture solution of 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indole-3-carboxaldehyde (350 mg) obtained in Example 25-(1), 4-(difluoromethoxy)benzeneboronic acid (399 mg), (acetylacetonato)dicarbonylrhodium(I) (37 mg) and 1,1′-bis-(diphenylphosphino)ferrocene (79 mg) in H2O (3.6 ml)-1,2-dimethoxyethane (3.6 ml) was stirred at 80° C. under argon atmosphere for 18 hours. The reaction mixture was cooled to room temperature, and thereto was added water (10 ml). The mixture was extracted with ethyl acetate (20 ml) 3 times, and the combined organic layer was dried over magnesium sulfate followed by being filtered through an aminosilane-treated silica gel pad. The filtrate was evaporated under reduced pressure to give crude 4-(difluoromethoxy)phenyl 4-fluoro-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)indol-3-yl methanol, which was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935674B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-1d79e428b0d74a12bdcb8c1ac27f19f4 |
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| Source note | uspto-grants-2011_05 |
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