Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | L-Galactose, 6-deoxy-, 2,3,4,5-tetraacetate | HCID 14701098 | — |
| Reactant | Ethyl 3-(2-hydroxyphenyl)benzyloxyacetate | HCID 19958321 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 53850275 | HCID 53850275 | 61% |
Reaction Steps
Part C: Ethyl 3-(2-hydroxyphenyl)benzyloxyacetate (0.85 g, 2.97 mmol) was dissolved in 1,2-dichloroethane (25 ml) in a dry 50 ml flask. L-Fucose tetraacetate (1.97 g, 5.94 mmol) was added in one portion, then boron trifluoride etherate (1.86 ml, 14.84 mmol) was added slowly. The mixture was stirred under nitrogen overnight at room temperature then mixed with water (50 ml). The organic material was separated and the aqueous portion was extracted with dichloromethane (3×5 ml). The extracts were combined with the original organic fraction, dried (MgSO4) then concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, gradient elution hexane to 3:1 hexane/ethyl acetate) which provided 1.0 g (61%) of ethyl 3-(2-(2,3,4-tri-O acetyl-α-L-fucopyranosyloxy)phenyl)benzyloxyacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05622937 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-8b24044829134d7eb2fa964c882a9cff |
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| Source note | uspto-grants-1997_04 |
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