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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487514Generated: October 28, 2026

Pyridine → HCID 12540017, compound

https://huagongshe.com/reaction/487514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChlorineHCID 24526—
Reactant1,1,1-Trichloro-N-(trimethylsilyl)silanamineHCID 12540015—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 12540017HCID 1254001775%

Reaction Steps

In accordance with L. P. Filonenko and A. M. Pinchuk in J. Gen. Chem. USSR 49, 302 (1979), 13.8 g (0.063 mol) compound A1 and 5.1 ml (0.063 mol) pyridine are initially introduced into a reaction vessel in 180 ml carbon tetrachloride. 5 g (0.141 mol) chlorine are condensed at -40° C. and transferred to the reaction vessel. After stirring for 4 hours, the precipitate is filtered off and washed and the solvent is distilled off from the combined filtrates. Subsequent fractionation leads to 16.4 g of the yellowish liquid A2 in a yield of 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296211
Source datasetuspto-grants-1994_03
ORD IDord-eeac356d85f141fc9f6d520292b5451c
Source noteuspto-grants-1994_03