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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400294Generated: October 27, 2026

Sodium Thiosulfate → 4-(phenyl-2-thienylmethyl)Pyridine

https://huagongshe.com/reaction/400294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant(Phenyl)-pyrid-4-yl-(thien-2-yl)methanolHCID 15525589—
SolventAcetonitrileHCID 6342—
Product4-(phenyl-2-thienylmethyl)PyridineHCID 15525585—

Reaction Steps

NAI (2.27 g, 16.0 mmol) and Me3Sicl (2.02, 16.0 mmol) were stirred in CH3CN (70 mL) at 0° C. (Phenyl)-pyrid-4-yl-(thien-2-yl)methanol (0.534 g, 2.00 mmol (Example 93)) was added at 0° C. and the resulting solution was stirred over night at room temperature. Na2S2O3 (sat., 20 mL) was added and the two phase system was stirred 5 minutes. The phases were separated and the organic layer was dried (MgSO4), filtered and evaporated. The resulting crystals were dissolved in CH2Cl2 (30 mL), the solution was washed with NaHCO3 (30 mL, sat.) and H2O (30 mL), dried (MgSO4) and evaporated yielding 0.41 g which was recrystallized in diisopropyl ether giving 0.22 g (43.8%) of the pure title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05827501
Source datasetuspto-grants-1998_10
ORD IDord-dd4992cda33d43fc886e61ed003e2b5f
Source noteuspto-grants-1998_10