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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168001Generated: November 4, 2026

tert-Butyldimethylsilyl trifluoromethanesulphonate → HCID 53920169, compound

https://huagongshe.com/reaction/1168001

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
ReactantSodium BicarbonateHCID 516892—
SolventPyridineHCID 1049—
SolventHexaneHCID 8058—
ProductHCID 53920169HCID 5392016998%

Reaction Steps

To a stirred solution of triethylsilyloxy keto diol 6 (883 mg, 2.31 mmol) in 35 mL of pyridine under nitrogen at 0° C. was added dropwise 0.485 mL (2.771 mmol) of TBSOTf. The solution was then warmed to room temperature. After 2 h at room temperature, the solution was diluted with 100 mL of hexane and poured into 150 mL of a saturated aqueous NaHCO3 solution. The organic layer was separated, and the aqueous layer was extracted with two 100 mL portions of hexane. The organic layers were combined, and washed with 50 mL of a 10% aqueous CuSO4 solution followed by 20 mL of H2O, and dried over anhydrous Na2SO4. Removal of the solvent followed by flash chromatography purification (2.5% EtOAc/hexane) to give 1.122 g of t-butyldimethylsilyloxy ketone 7 (98% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620950B2
Source datasetuspto-grants-2003_09
ORD IDord-10a4b841528f46b1bebb6c9c43ce7744
Source noteuspto-grants-2003_09