HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72610Generated: October 29, 2026
Boron trifluoride → HCID 67115776, compound
https://huagongshe.com/reaction/72610
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | (3R,4S,5S,6R)-2-(4-bromo-3-((2,3-dihydrobenzo[b][1,4]dioxin-6-yl)meth yl)phenyl)-6-(hydroxymethyl)-2-methoxytetrahydro-2H-pyran-3,4,5-triol | HCID 58340876 | — |
| Solvent | Acetonitrile methylene chloride | HCID 21877088 | — |
| Product | HCID 67115776 | HCID 67115776 | 106.4% |
Reaction Steps
To a stirred solution of (3R,4S,5S,6R)-2-[4-bromo-3-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-phenyl]-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3,4,5-triol (28.4 g, 57.1 mmol) in acetonitrile-dichloromethane 1:1 (250 mL) was added triethylsilane (36.5 mL, 228.4 mmol) and boron trifluoride diethyletharate complex (14.1 mL, 114.2 mmol) at 10° C. After stirring for 4 h at 10° C., the reaction was quenched with saturated aqueous sodium bicarbonate (˜100 mL). The organic layer was separated, and the aqueous layer was extracted with ethyl acetate (3×150 mL). The organic layers were combined and dried over sodium sulfate, concentrated to furnish (3R,4R,5S,6R)-2-[4-bromo-3-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-phenyl]-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol (28.4 g). Crude product was used for next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828951B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-b9cc327d763d40b6803211965e66990a |
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| Source note | uspto-grants-2014_09 |
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