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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175233Generated: October 31, 2026

Boron trifluoride etherate → HCID 57684690, compound

https://huagongshe.com/reaction/1175233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 57684684HCID 57684684—
SolventAcetonitrile methylene chlorideHCID 21877088—
ProductHCID 57684690HCID 57684690—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-2-(4-chloro-3-(4-vinylbenzyl)phenyl)tetrahydro-2H-pyran-2-ol (intermediate AN) (350 mg) in 4 mL of CH2Cl2:CH3CN (1:1) at −15° C. was added Et3SiH (0.146 mL), followed by BF3.Et2O (0.09 mL). During the period of addition, the temperature was maintained at approximately −5° C. to −10° C. The stirred solution was allowed to warm to 0° C. over 5 h. The reaction was monitored by TLC, and after the starting material was consumed, the reaction was quenched by addition of saturated aqueous NaHCO3. The solvent was removed under reduced pressure. The residue was then dissolved in a mixture of 40 mL of ethyl acetate and water (1:1). After separation of the organic layer, the aqueous phase was extracted 2× with 20 mL of ethyl acetate. The organic phases were combined and washed with brine and water before drying over Na2SO4. Concentration of the solution yielded a yellow gel, which was purified by preparative TLC to obtain pure intermediate AO (100 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838499B2
Source datasetuspto-grants-2010_11
ORD IDord-b01ab4c4bab14ab48d4e4009ef03bf50
Source noteuspto-grants-2010_11