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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599349Generated: November 3, 2026

Pyridinium → HCID 85303357, compound

https://huagongshe.com/reaction/1599349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridiniumHCID 4989215—
ReactantHCID 86751408HCID 86751408—
SolventEthanolHCID 702—
ProductHCID 85303357HCID 8530335792%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of the alkyne 12b (526 mg, 457 μmol) in absolute ethanol (6.0 mL) was added pyridinium p-toluenesulfanate (273 mg, 1.09 mmol) in one portion. The reaction mixture was stirred at 55° C. overnight (~14 h). The solvent was removed in vacuo and the residue was dissolved in ethyl acetate (50 mL). The organic solution was washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude product was purified by MPLC (3:1 hexane:ethyl acetate) to give the alcohol 14 (387 mg, 92%); IR (neat, thin layer): 3405, 3070, 3048, 2935, 2858, 1963, 1893, 1827, 1589, 1507, 1471, 1428, 1365, 1228, 1155, 1002, and 823 cm-1 ; Anal. Calcd for C58 H74O6Si2 : C, 75.44%; H, 8.08%. Found: C, 75.16%; H, 7.89%; tlc: Rf =0.14 in 3:1 hexane:ethyl acetate; [α]RTD =-7.9°, c=5.47 in ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739358
Source datasetuspto-grants-1998_04
ORD IDord-a894e5cd021c429696d97df1078cca72
Source noteuspto-grants-1998_04